A New Compound Heterozygous Mutation (W17X, 436+5G→T) in...

Journal of Clinical Endocrinology & Metabolism 1998 / 01 Vol. 83; Iss. 1

A New Compound Heterozygous Mutation (W17X, 436+5G→T) in the Cytochrome P450c17 Gene Causes 17α-Hydroxylase/17,20-Lyase Deficiency

Suzuki, Yukie, Nagashima, Tomohisa, Nomura, Yoko, Onigata, Kazumichi, Nagashima, Kanji, Morikawa, Akihiro
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
83
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.83.1.4516
Date:
January, 1998
File:
PDF, 388 KB
english, 1998
Conversion to is in progress
Conversion to is failed