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pro vyhledávání: '"Nilza Nei Torres"'
Autor:
Tarcísio André Amorim de Carvalho, Izabel Cristina Neves de Souza, France Keiko Nascimento Yoshioka, Milena Coelho Fernandes Caldato, Nilza Nei Torres, Lena Stilianidi Garcia, João Farias Guerreiro
Publikováno v:
Genetics and Molecular Biology, Vol 31, Iss 3, Pp 626-631 (2008)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (P450c21, CYP21) accounts for about 95% of all CAH cases. The incidence of CYP21 gene mutations has been extensively studied in the last years, but in Brazil it has been investigat
Externí odkaz:
https://doaj.org/article/ed43b6e229404e93a7340c0d0e0f8897
