Author:
Takayama Kazuko,Mitsuhashi Satomi,Shin Je-Young,Tanaka Rieko,Fujii Tatsuya,Tsuburaya Rie,Mukaida Souichi,Noguchi Satoru,Nonaka Ikuya,Nishino Ichizo
Funder
Health and Labour Sciences Research Grants for Comprehensive Research on Persons with Disabilities
Practical Research Project for Rare/Intractable Diseases
JSPS KAKENHI
Neurological and Psychiatric Disorders from the National Center of Neurology and Psychiatry
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference7 articles.
1. Mutations in MEGF10, a regulator of satellite cell myogenesis, cause earlyonset myopathy, areflexia, respiratory distress and dysphagia (EMARDD);Logan;Nat Genet,2011
2. Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD);Pierson;Neuromuscul Disord,2013
3. Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores;Boyden;Neurogenetics,2012
4. Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy;Mitsuhashi;FEBS Lett,2013
5. Megf10 regulates the progression of the satellite cell myogenic program;Holterman;J Cell Biol,2007
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