Publication | Closed Access
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
180
Citations
9
References
1995
Year
Developmental BiologyMendelian DisorderSkeletal MuscleGenetic DisorderMedicineGeneticsPhysiologyDegenerative DiseaseCytoskeletonClinical PhenotypeNeuromuscular PathologyNeuromusculoskeletal DisorderCongenital Muscular Dystrophy
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