peau (1) protéine (1) mutation (1) perte (1) gène (1) classification (1) Diagnosis (1) Decay (1) Methods (1) Identification (1) Cases (1) Phenotype (1) Reverse transcriptase (1) Genes (1) Antisense DNA (1) Polymerase chain reaction (1) Work (1) Skin (1) Secretion (1) Patients (1) Muscular dystrophy (1) Muscles--Diseases (1) Life (1) Identification (1) Helix (Mollusks) (1) Extracellular matrix (1) Glycine (1) Fibroblasts (1) Diagnosis (1) Design (1)