Gene table: search width pubmed_id = 10958653


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myofibrillar myopathy 3 (Formerly LGMD1A) - (AD)
1.24
10958653
1598902
MYOT (5q31)
Myotilin
* Myofibrillar myopathy, myotilin related - MFM3
* Spheroid body myopathy
* Muscular dystrophy, Limb-Girdle, type 1A - LGMD1A