A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A) - Concepedia

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A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A)

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Citations

20

References

2011

Year

Peter Reilich, Sabine Krause, Nicolai Schramm, Ursula Klutzny, Stefanie Bulst, Barbara Zehetmayer, Peter Schneiderat, Maggie C. Walter, Benedikt Schoser, Hanns Lochmüller

Journal of Neurology

Novel MutationRare DiseasesDevelopmental BiologyMendelian DisorderSkeletal MuscleGenetic DisorderGeneticsMyotilin GeneDisease Gene IdentificationSevere FormMedicine

References

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