Gene table: search width pubmed_id = 9245996


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

protein
All allelic disease phenotypes - locus/disease symbols
Muscular dystrophy, limb-girdle, autosomal recessive 7 - (AR)
1.31
10655062
9245996
TCAP (17q12)
Telethonin
* Dilated cardiomyopathy, 1N
* Congenital musuclar dystrophy with telethonin defect
* Hypertrophic cardiomyopathy related to TCAP - CMH25
* Muscular dystrophy, limb-girdle, type 2G - LGMD2G