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Autor:
M. A. Nikitina, E. Yu. Bragina, M. S. Nazarenko, N. G. Zhukova, D. E. Gomboeva, K. F. Nurzhanova, N. V. Tsentr, V. M. Alifirova
Publikováno v:
Бюллетень сибирской медицины, Vol 19, Iss 4, Pp 235-240 (2021)
Huntington’s disease (HD) is an autosomal dominant progressive neurodegenerative disease. Its molecular cause is a cytosine-adenine-guanine (CAG) trinucleotide repeat dynamic expansion in the huntingtin (HTT) gene. Alleles with 36–39 CAG-repeats
Externí odkaz:
https://doaj.org/article/e893760408d04c12a8654aceb7524b6c
