C.O.6 Complete genetic analysis by whole exome sequencing of a cohort with centronuclear myopathy identifies titin gene mutations

Journal article

Peer reviewed

Pankaj B. Agrawal, K. Schmitz, Elizabeth T. DeChene, O. Ceyhan, M. Mercier, Marissa G. Viola, Kyriacos Markianos and Alan H. Beggs

Neuromuscular Disorders, Vol.22(9), p.840

2012

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url

https://lens.org/005-095-218-841-715View

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https://www.sciencedirect.com/science/article/abs/pii/S0960896612003100View

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Citation topics: 1 Clinical & Life Sciences; 1.189 Genome Studies; 1.189.597 BRCA1
Web Of Science research areas: Clinical Neurology; Neurosciences
ESI research areas: Neuroscience & Behavior

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Source: InCites

Title: C.O.6 Complete genetic analysis by whole exome sequencing of a cohort with centronuclear myopathy identifies titin gene mutations
Creators: Pankaj B. Agrawal - Boston Children's Hospital
K. Schmitz - Boston Children's Hospital
Elizabeth T. DeChene - Boston Children's Hospital
O. Ceyhan - Boston Children's Hospital
M. Mercier - Boston Children's Hospital
Marissa G. Viola - Boston Children's Hospital
Kyriacos Markianos - Boston Children's Hospital
Alan H. Beggs - Boston Children's Hospital
Publication Details: Neuromuscular Disorders, Vol.22(9), p.840
Publisher: Elsevier BV; Netherlands
Academic Unit: Miller School of Medicine; UMMG Dept of Pediatrics - Neonatology; UMMG Department of Pediatrics
Resource Type: Journal article
Record Identifier: 991031926697702976