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4. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity. Sabatelli M, Mignogna T, Lippi G, Servidei S, Zollino M, Padua L, Lo Monaco M, De Armas L, Mereu ML, Tonali P. Am J Med Genet; 1998 Jan 23; 75(3):309-13. PubMed ID: 9475604 [Abstract] [Full Text] [Related]
5. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation]. Adachi T, Imaoka K, Shirasawa A, Yamaguchi S, Kobayashi S. Rinsho Shinkeigaku; 1998 Dec 23; 38(12):1037-41. PubMed ID: 10349345 [Abstract] [Full Text] [Related]
12. [Optic atrophy, type I diabetes and neurosensory hearing loss: a family syndrome]. Bujara K, Burck U, Dreyer M, Koepp P, Herberhold C. Klin Monbl Augenheilkd; 1982 Jun 23; 180(6):559-62. PubMed ID: 6890123 [No Abstract] [Full Text] [Related]
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20. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R. Brain; 2003 Dec 23; 126(Pt 12):2682-92. PubMed ID: 14506069 [Abstract] [Full Text] [Related] Page: [Next] [New Search]