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Qualitative or quantitative defects of gamma-sarcoglycan

MONDO:0016143

Also known as: gamma-sarcoglycanopathy

4 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive limb-girdle muscular dystrophy type 2C (4)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Human disease (14) Hereditary neurological disease (5) Sarcoglycanopathy (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Qualitative or quantitative protein defects in neuromuscular diseases (0)
Trials to join now! 1 Not yet finished but already full! 3
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  • Major study aims to better measure muscular dystrophy progression

    Knowledge-focused Recruiting now

    This 24-month observational study will follow up to 1000 people with certain types of muscular dystrophy (LGMD, DM2, and late-onset Pompe disease) aged 6-50. Researchers want to see if specific physical tests, like the North Star Assessment and a 100-meter walk, are good ways to …

    Sponsor: Virginia Commonwealth University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:57 UTC

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