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Paper Details

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.
Neurogenetics
6
2021
Author NameAffiliation
Rita HorvathUniversity of Cambridge
Hanns Lochm??llerChildren's Hospital of Eastern Ontario Research Institute
Hanns Lochm??llerThe Ottawa Hospital
Hanns Lochm??llerBrain and Mind Research Institute, University of Ottawa
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