Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies-Reference-Cited by-同舟云学术

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

Published:2014-07 Issue:7 Volume:24 Page:624-633
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kayman-Kurekci Gulsum,Talim Beril,Korkusuz Petek,Sayar Nilufer,Sarioglu Turkan,Oncel Ibrahim,Sharafi Parisa,Gundesli Hulya,Balci-Hayta Burcu,Purali Nuhan,Serdaroglu-Oflazer Piraye,Topaloglu Haluk,Dincer Pervin

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

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4. Clinical and molecular genetic spectrum of autosomal dominant Emery–Dreifuss muscular dystrophy due to mutations of the lamin A/C gene;Bonne;Ann Neurol,2000

5. Distal myopathies—new genetic entities expand diagnostic challenge;Udd;Neuromuscul Disord,2012

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