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Results 1 - 4 of 4 for Muscular "dystrophy," "limb-girdle," autosomal recessive 26
  1. ... individuals eventually require wheelchair assistance. DYSF_HUMAN dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) dystrophy-associated fer-1-like 1 fer-1- ...
  2. ... ClinVar Allamand V, Guicheney P. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 ...
  3. ... to the signs and symptoms of LAMA2-related muscular dystrophy. LAMA2 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
  4. ... myopathy, and atypical dysferlinopathies. Hum Mutat. 2005 Aug;26(2):165. doi: 10.1002/humu.9355. Citation on PubMed Nilsson MI, Laureano ML, Saeed M, Tarnopolsky MA. Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for ...