Gene table: search width pubmed_id = 17676042


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Centronuclear myopathy, related to BIN1, recessive - (AR)
3.22
17676042
BIN1 (2q14)
Amphiphysin
* Centronuclear myopathy, related to BIN1, recessive
* Centronuclear myopathy, related to BIN1, dominant