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

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

Book ID: 111995302
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 231 KB
Volume: 158A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.35495

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