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Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria

✍ Scribed by David R. Murdock; Gary D. Clark; Matthew N. Bainbridge; Irene Newsham; Yuan-Qing Wu; Donna M. Muzny; Sau Wai Cheung; Richard A. Gibbs; Melissa B. Ramocki

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 992 KB
Volume: 155
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.34165

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