Concepedia

Japanese multiple epidermal growth factor 10 (MEGF10) myopathy with novel mutations: A phenotype–genotype correlation

K. Takayama, Satomi Mitsuhashi, Je-Young Shin, Rieko Tanaka, Tatsuya Fujii, R. Tsuburaya, Souichi Mukaida, S. Noguchi, Ikuya Nonaka, Ichizo Nishino

Neuromuscular Disorders · 2016 · 23 citations · 7 references

DOI

Concepts

References

7

MEGF10 and MEGF11 mediate homotypic interactions required for mosaic spacing of retinal neurons

Jeremy N. Kay, Monica W. Chu, Joshua R. Sanes · Nature · 2012 · 225 citations

, , +13

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

Clare V. Logan, Barbara Lucke, Caroline Pottinger et al. · Nature Genetics · 2011 · 113 citations

, , +13

Megf10 regulates the progression of the satellite cell myogenic program

Chet E. Holterman, Fabien Le Grand, Shihuan Kuang et al. · The Journal of Cell Biology · 2007 · 99 citations · Full text

, , +16

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

Steven E. Boyden, Lane J. Mahoney, Genri Kawahara et al. · Neurogenetics · 2012 · 83 citations · Full text

, , +17

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)

Tyler Mark Pierson, Thomas C. Markello, John Accardi et al. · Neuromuscular Disorders · 2013 · 27 citations · Full text

, , +17