Phenotype (4) Human beings (4) protéine (3) adulte (3) Series (3) Patients (3) Adulthood (3) Patients (3) adulte (3) région (2) mutation (2) analyse (2) gène (2) ADN (2) maladie (2) Causes (2) Cases (2) Genes (2) Mice (2) Head (2) Gene expression (2) Expression (2) Dystrophy (2) DNA (2) Animals (2) Cases (2) Optical coherence tomography (2) Disabilities (2) Regions (2) Analysis (2)