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Congenital muscular dystrophy 1B
- ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov CONGENITAL MYOPATHY 1B, AUTOSOMAL RECESSIVE; CMYO1B CONGENITAL MYOPATHY 3 WITH RIGID ...
- ... ClinicalTrials.gov CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; ... HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE; CHN1 CHARCOT-MARIE-TOOTH ...