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Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene

ChromatinMendelian DisorderGenetic DisorderGeneticsNonsense Y259xNuclear Envelope AlterationsMolecular GeneticsDisease Gene IdentificationLamin A/c GeneMedicineCell BiologyVariant Interpretation