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GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia [CMT1A] [CMT1B] [CMT1F] [CMT2A2] [CMT2B1] [CMT2E] [CMT2F] [CMT2J] [CMT4A] [CMT4B1] [CMT4C] [CMT4E] [CMT4F] [CMT4H] [CMT4J] [CMTDIB] [CMTRIA] [CMTX5] [CMTX] Charcot-Marie-Tooth disease Neuropathy, hereditary motor and sensory [Clinical features: hereditary motor and sensory neuropathy; progressive distal wasting; loss of reflexes in the muscles of the legs] |
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Edited by Aldo Campana,
August 21, 2012
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