Variant: rs104894787 

    present in Gene: DMD
    present in Chromosome: X
    Position on Chromosome: 31178784
    Alleles of this Variant: G/A

rs104894787 in DMD gene and Dmd-Associated Dilated Cardiomyopathy PMID 21396098 2011 Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.

PMID 19367636 2009 Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.

PMID 25612904 2015 A comprehensive database of Duchenne and Becker muscular dystrophy patients (0-18 years old) in East China.

PMID 18652600 2008 Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes.

PMID 21525508 2011 How does type 1 diabetes develop?: the notion of homicide or β-cell suicide revisited.

PMID 15351422 2004 The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.

PMID 1549596 1992 Point mutations in the dystrophin gene.

PMID 18583217 2008 Small mutations of the DMD gene in Taiwanese families.