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Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria.
Murdock, David R; Clark, Gary D; Bainbridge, Matthew N; Newsham, Irene; Wu, Yuan-Qing; Muzny, Donna M; Cheung, Sau Wai; Gibbs, Richard A; Ramocki, Melissa B.
Affiliation
  • Murdock DR; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Am J Med Genet A ; 155A(9): 2071-7, 2011 Sep.
Article in En | MEDLINE | ID: mdl-21834044
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Malformations of Cortical Development / Exome / Nerve Tissue Proteins Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Malformations of Cortical Development / Exome / Nerve Tissue Proteins Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Document type: Article Affiliation country: United States