RS2114697790 LAMA2
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Associated Conditions
See cases
Merosin deficient congenital muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal recessive 23
See cases
Merosin deficient congenital muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal recessive 23
Other Variants in LAMA2