New Step by Step Map For Muscular dystrophy treatment

Limb-girdle muscular dystrophies can both be autosomal dominant (single gene defect on a chromosome from both parent or a person copy of a mutant gene and a single normal gene, often known as form one LGMD) or autosomal recessive (a defect or mutation around the gene in the chromosome of each guardian is needed, called kind two LGMD). the sort 2 LG

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