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4. [A case of hereditary hypertrophic interstitial neuropathy accompanied with cataract, neurogenic deafness and hand tremor]. Kaseda Y; Kuroda Y; Oda K; Shibasaki H; Ohnishi A Rinsho Shinkeigaku; 1986 Jan; 26(1):55-8. PubMed ID: 3009070 [No Abstract] [Full Text] [Related]
5. A new variety of hereditary sensory neuropathy. Robinson GC; Jan JE; Miller JR Hum Genet; 1977 Feb; 35(2):153-61. PubMed ID: 191348 [TBL] [Abstract][Full Text] [Related]
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9. Clinical and pathological features of an autosomal recessive neuropathy. Bouldin TW; Riley E; Hall CD; Swift M J Neurol Sci; 1980 Jun; 46(3):315-23. PubMed ID: 6247456 [TBL] [Abstract][Full Text] [Related]
10. A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study. Nelson I; Hanna MG; Alsanjari N; Scaravilli F; Morgan-Hughes JA; Harding AE Ann Neurol; 1995 Mar; 37(3):400-3. PubMed ID: 7695240 [TBL] [Abstract][Full Text] [Related]
11. Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23. Bomont P; Watanabe M; Gershoni-Barush R; Shizuka M; Tanaka M; Sugano J; Guiraud-Chaumeil C; Koenig M Eur J Hum Genet; 2000 Dec; 8(12):986-90. PubMed ID: 11175288 [TBL] [Abstract][Full Text] [Related]
12. Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant. Hamiel OP; Raas-Rothschild A; Upadhyaya M; Frydman M; Sarova-Pinhas I; Brand N; Passwell JH J Pediatr; 1993 Sep; 123(3):431-4. PubMed ID: 8355122 [TBL] [Abstract][Full Text] [Related]
13. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352 [TBL] [Abstract][Full Text] [Related]