Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
SHINAGAWA, Takashi, HORIKAWA, Reiko, ISOJIMA, Tsuyoshi, NAIKI, Yasuhiro, TANAKA, Toshiaki, KATSUMATA, NoriyukiVolume:
54
Year:
2007
Language:
english
Journal:
Endocrine Journal
DOI:
10.1507/endocrj.k07-028
File:
PDF, 213 KB
english, 2007