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An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathologyDegenerative DiseaseDisease Gene IdentificationMild Mental RetardationPomt1 GeneMedicineMonogenic DisordersWalker–warburg Syndrome