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A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients

Crossref DOI link: https://doi.org/10.1007/s10048-021-00658-1

Published Online: 2021-08-01

Published Print: 2021-10

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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