and Evolution // Quarterly Review of Biology, 2017, 92. P. 1–38.
377
J. Klein. Woody Guthrie: A Life. Dell Publishing/Random House, Inc.: New York, 1980.
378
Woody Guthrie. This Land is Your Land, 1944. URL: https://www.youtube.com/watch?v=wxiMrvDbq3s.
379
K. B. Bhattacharyya. The story of George Huntington and his disease // Annals of Indian Academy of Neurology, 2016, 19. P. 25–28.
380
G. Huntington. On Chorea // Medical and Surgical Reporter of Philadelphia, 1872, 26. P. 317–321.
381
J. Huddleston and E. E. Eichler. An Incomplete Understanding of Human Genetic Variation // Genetics, 2016, 202. P. 1251–1254.
382
Genomes Project Consortium. A global reference for human genetic variation // Nature, 2015, 526. P. 68–74.
383
G. Mendel. Versuche über Pflanzenhybriden // Verhandlungen des naturforschenden Vereines in Brünn, 1866, IV. P. 3–47.
384
R. Marantz Henig. The Monk in the Garden: The Lost and Found Genius of Gregor Mendel, the Father of Genetics. Houghton Mifflin: Boston, 2001.
385
E. W. Crow and J. F. Crow. 100 Years Ago: Walter Sutton and the Chromosome Theory of Heredity // Genetics, 2002, 160. P. 1–4.
386
C. D. Darlington. Meiosis in perspective // Philosophical Transactions of the Royal Society of London, 1977, B277. P. 185–189.
387
N. S. Wexler. Huntington’s Disease: Advocacy Driving Science // Annual Review of Medicine, vol. 63, ed. C. T. Caskey, C. P. Austin and J. A. Hoxie, 2012. P. 1–22.
388
J. F. Gusella et al. A Polymorphic DNA Marker Genetically Linked to Huntington’s Disease // Nature, 1983, 306. P. 234–238.
389
N. S. Wexler. Huntington’s Disease: Advocacy Driving Science // Annual Review of Medicine, vol. 63, ed. C. T. Caskey, C. P. Austin and J. A. Hoxie, 2012. P. 1–22.
390
F. Saudou and S. Humbert. The Biology of Huntingtin // Neuron, 2016, 89. P. 910–926.
391
H. Paulson. Repeat expansion diseases // Handbook of clinical neurology, 2018, 147. P. 105–123.
392
M. Jimenez-Sanchez et al. Huntington’s Disease: Mechanisms of Pathogenesis and Therapeutic Strategies // Cold Spring Harbor Perspectives in Medicine, 2017, 7.
393
I. Ionis Pharmaceuticals. Ionis Pharmaceuticals Licenses IONIS-HTT Rx to Partner Following Successful Phase 1/2a Study in Patients with Huntington’s Disease, 2017. URL: http://ir.ionispharma.com/news-releases/news-release-details/ionis-pharmaceuticals-licenses-ionis-htt-rx-partner-following.
394
D. Kwon. Failure of genetic therapies for Huntington’s devastates community // Nature, 2021, 180. P. 593.
395
Z. Li et al. Allele-selective lowering of mutant HTT protein by HTT — LC3 linker compounds // Nature, 2019, 575. P. 203–209.
396
D. Grady. Haunted by a Gene // New York Times [Online], 2020. URL: https://www.nytimes.com/2020/03/10/health/huntingtons-disease-wexler.html.
397
Genetics Home Reference. Fumarase deficiency, 2020. URL: https://ghr.nlm.nih.gov/condition/fumarase-deficiency.
398
J. Dougherty. Forbidden Fruit // Phoenix New Times [Online], 2005. URL: https://www.phoenixnewtimes.com/news/forbidden-fruit-6438448.
399
Ibid.
400
M. Oswaks. Tiny Tombstones: Inside the FLDS Graveyard for Babies Born from Incest // Vice.com [Online], 2016. URL: https://www.vice.com/en_us/article/qkgymp/tiny-tombstones-inside-the-flds-graveyard-forbabies-born-from-incest.
401
J. Dougherty. Forbidden Fruit // Phoenix New Times [Online], 2005. URL: https://www.phoenixnewtimes.com/news/forbidden-fruit-6438448.
402
R. Sanchez. Fort Knox has nothing on polygamist compound // Anderson Cooper Blog 360° [Online], 2006. URL: http://edition.cnn.com/CNN/Programs/anderson.cooper.360/blog/2006/05/fort-knox-has-nothing-on-polygamist.html.
403
J. Hollenhorst. Sex banned until Warren Jeffs’ prison walls crumble, FLDS relatives say, 2011. URL: https://www.deseret.com/2011/12/30/20391030/sex-banned-until-warren-jeffs-prison-walls-crumble-flds-relatives-say.
404
T. K. Danovich. The Forest Hidden Behind the Canyons, 2019. URL: https://www.theringer.com/2019/6/24/18692816/flds-short-creek-polygamy-feature.
405
L. Yengo et al. Extreme inbreeding in a European ancestry sample from the contemporary UK population // Nature Communications, 2019. P. 10.
406
H. Hamamy. Consanguineous marriages: Preconception consultation in primary health care settings // Journal of Community Genetics, 2012, 3. P. 185–192.
407
N. Al-Dewik et al. Clinical genetics and genomic medicine in Qatar // Molecular Genetics and Genomic Medicine, 2018, 6. P. 702–712.
408
P. K. Joshi et al. Directional dominance on stature and cognition in diverse human populations // Nature, 2015, 523. P. 459–462.
409
C. R. Scriver. Human genetics: Lessons from Quebec populations // Annual Review of Genomics and Human Genetics, 2001, 2. P. 69–101.
410
A. M. Laberge et al. A «Fille du Roy» introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians // American Journal of Human Genetics, 2005, 77. P. 313–317.
411
N. J. R. Fagundes et al. How strong was the bottleneck associated to the peopling of the Americas? New insights from multilocus sequence data // Genetics and Molecular Biology, 2018, 41. P. 206–214.
412
M. N. Leathlobhair et al. The evolutionary history of dogs in the Americas // Science, 2018, 361. P. 81–85.
413
Z. Y. Gao et al. An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans // Genetics, 2015, 199. P. 1243–1254.
414
V. Grech et al. Unexplained differences in sex ratios at birth in Europe and North America // British Medical Journal, 2002, 324. P. 1010, 1011.
415
E. I. Rogaev et al. Genotype Analysis Identifies the Cause of the «Royal Disease» // Science, 2009, 326. P. 817.
416
S. M. Carr. Hemophilia in Victoria pedigree, 2012. URL: https://www.mun.ca/biology/scarr/Hemophilia_in_Victoria_pedigree.jpg.
417
E. I. Rogaev et al. Genomic identification in the historical case of the Nicholas II royal family // Proceedings of the National Academy of Sciences of the USA, 2009, 106. P. 5258–5263.
418
E. I. Rogaev et al. Genotype Analysis
