RS143638361 LAMA2
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Associated Conditions
Merosin deficient congenital muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal recessive 23
LAMA2-related muscular dystrophy
Primary dilated cardiomyopathy
Merosin deficient congenital muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal recessive 23
LAMA2-related muscular dystrophy
Primary dilated cardiomyopathy
Other Variants in LAMA2