Publication | Closed Access
Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene
39
Citations
13
References
2001
Year
Large Japanese FamilyMiyoshi MyopathyMendelian DisorderGenetic DisorderGeneticsDysferlin GenePathologyMolecular GeneticsDisease Gene IdentificationMedicineClinical Genetics
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