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Autosomal dominant intermediate "Charcot-Marie-Tooth" disease
- ... SENSORY, RUSSE TYPE; HMSNR NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE; CHN1 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D; CMTDID CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE ...
- Causes of Charcot-Marie-Tooth Disease (CMT) (Muscular Dystrophy Association)MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
- ... in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances ( ...
