Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B-Reference-Cited by-同舟云学术

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Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

Published:2010-11-18 Issue:1 Volume:32 Page:E1976-E1984
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ho Gladys,Yonezawa Atsushi,Masuda Satohiro,Inui Ken-ichi,Sim Keow G.,Carpenter Kevin,Olsen Rikke K.J.,Mitchell John J.,Rhead William J.,Peters Gregory,Christodoulou John

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21399/fullpdf

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