Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2q

Alias:
Autosomal Recessive Limb-Girdle Muscular Dystrophy Due to Plectin Deficiency
Muscular Dystrophy, Limb-Girdle, Type 2q
Lgmd2q
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2q, also known as autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency, is related to muscular dystrophy, limb-girdle, autosomal recessive 17 and epidermolysis bullosa simplex 5d, generalized intermediate, autosomal recessive, and has symptoms including generalized muscle weakness An important gene associated with Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2q is PLEC (Plectin). Affiliated tissues include lung and skin, and related phenotype is muscle.
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Basic Information

Inheritance
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Related Gene
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Reference
MALACARDS
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Unknown
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17
104
23

Medical Symptom

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Gene & Mutation

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References Literature

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