Gene table: search width pubmed_id = 9620781


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

protein
All allelic disease phenotypes - locus/disease symbols
Myotonic dystrophy type 2 (proximal myotonic myopathy) - (AD)
6.2
11486088
9620781
CNBP (3q21.3)
Cellular nucleic acid-binding protein
* Proximal myotonic myopathy - PROMM
* Myotonic dystrophy, type 2 - DM2