HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

autosomal dominant Charcot-Marie-Tooth disease with pyramidal features

merge Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant; and Peroneal muscular atrophy with pyramidal features, autosomal dominant wtih Hereditary Autosomal Dominant Spastic Paraplegia. Merge Hereditary motor and sensory neuropathy 5 and HMSN 5 with Spastic Paraplegia, Hereditary
Also Known As:
Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant; HMSN 5; Hereditary motor and sensory neuropathy 5; Peroneal muscular atrophy with pyramidal features, autosomal dominant
Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results