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Am J Med Genet A. 2007 Dec 1;143A(23):2835-7.

A novel VPS33B mutation in an ARC syndrome patient presenting with osteopenia and fractures at birth.

Author information

1
Division of Pediatric Endocrinology, Department of Pediatrics, King Faisal Specialist Hospital and Research Centre-Jeddah, Kingdom of Saudi Arabia. dtaha@kfshrc.edu.sa
PMID:
17994566
DOI:
10.1002/ajmg.a.32051
[Indexed for MEDLINE]

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