| Document Date: 2015-02-22 11:07:14 Open Document File Size: 364,29 KBShare Result on Facebook
Country France / United States / United Kingdom / / Currency pence / / IndustryTerm manufacturing myelin protein zero / orthopedic devices / / MedicalCondition paralysis / Foot deformities / HMSN / X-linked disorder / Progressive muscle weakness / palsy / disease / common inherited neurological disorders / Marie-Tooth disease / Charcot-MarieTooth disease / Autosomal disorders / Charcot-Marie-Tooth disease / autosomal dominant disease / muscle weakness / hereditary motor / Dejerine-Sottas disease / hereditary neuropathy / X-linked dominant disease / severe muscle atrophy / cut / CMT experience tremor / peroneal muscular atrophy / rare disorder / disorder / Autosomal recessive disorders / demyelination / CMT disease / heterogenous genetic disease / chronic shortening / contractures / Nerve pain / scoliosis / disorders / / Organization U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES / DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Institutes of Health / / Person Howard Henry Tooth / Pierre Marie / Jean-Martin Charcot / / Product FS / / Technology genetic code / /
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