Novel intronic CYP21A2 mutation in a Japanese patient with...

Metabolism 2010 Vol. 59; Iss. 11

Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency

Noriyuki Katsumata, Takashi Shinagawa, Reiko Horikawa, Kaori Fujikura
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Volume:
59
Year:
2010
Language:
english
Pages:
5
DOI:
10.1016/j.metabol.2010.03.012
File:
PDF, 337 KB
english, 2010
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