Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation inAGXTand a terminal deletion of chromosome 2-Reference-Cited by-同舟云学术

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation inAGXTand a terminal deletion of chromosome 2

Published:2012-07-20 Issue:9 Volume:158A Page:2124-2130
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Tammachote Rachaneekorn,Kingsuwannapong Nelawat,Tongkobpetch Siraprapa,Srichomthong Chalurmpon,Yeetong Patra,Kingwatanakul Pornchai,Monico Carla G.,Suphapeetiporn Kanya,Shotelersuk Vorasuk

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35495/fullpdf

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