A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency

A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency

Bibliographic Details
Main Authors: Idkowiak, Jan, Randell, Tabitha, Dhir, Vivek, Patel, Pushpa, Shackleton, Cedric H. L., Taylor, Norman F., Krone, Nils, Arlt, Wiebke
Format: Online
Language:English
Published: Endocrine Society 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388247/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388247/

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