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Volumn 57, Issue 2 A, 1999, Pages 190-194

Hereditary motor and sensory neuropathy with congenital glaucoma: Report on a family

Author keywords

Autosomal recessive inheritance; Congenital glaucoma; Hereditary motor and sensory neuropathy

Indexed keywords

ADULT; ARTICLE; FEMALE; GENETICS; GLAUCOMA; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; PEDIGREE;

EID: 0033144993     PISSN: 0004282X     EISSN: None     Source Type: Journal    
DOI: 10.1590/S0004-282X1999000200004     Document Type: Article
Times cited : (9)

References (9)
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    • (1993) Peripheral Neuropathy, 3Ed. , pp. 1094-1136
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  • 2
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    • The clinical features of hereditary motor and sensory neuropathy types I and II
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    • (1980) Brain , vol.103 , pp. 259-280
    • Harding, A.E.1    Thomas, P.K.2
  • 3
    • 0031934267 scopus 로고    scopus 로고
    • Genetically determined neuropathies
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    • Reilly, M.M.1
  • 4
    • 0027491703 scopus 로고
    • Linkage of a locus (CMT4) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
    • Othmane KB, Hentati F, Lennon F, et al. Linkage of a locus (CMT4) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 1993;10:1625-1628.
    • (1993) Hum Mol Genet , vol.10 , pp. 1625-1628
    • Othmane, K.B.1    Hentati, F.2    Lennon, F.3
  • 5
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    • Localisation of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozigosity mapping and haplotype sharing
    • Bolino A, Brancolini V, Bono F, et al. Localisation of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozigosity mapping and haplotype sharing. Hum Mol Genet 1996;5:1051-1054.
    • (1996) Hum Mol Genet , vol.5 , pp. 1051-1054
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  • 6
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    • Homozygosity mapping of an autosomal recessive fdorm of demyelinating Charcot-Marie-tooth disease to chromosome 5123-q33
    • LeGuern E, Guilbot A, Kessali M, et al. Homozygosity mapping of an autosomal recessive fdorm of demyelinating Charcot-Marie-tooth disease to chromosome 5123-q33. Hum Mol Genet 1996;5:1685-1688.
    • (1996) Hum Mol Genet , vol.5 , pp. 1685-1688
    • LeGuern, E.1    Guilbot, A.2    Kessali, M.3
  • 7
    • 16044365767 scopus 로고    scopus 로고
    • Gene mapping of Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24
    • Kalaydjieva L, Hallmayer J, Chandler D, et al. Gene mapping of Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat Genet 1996;14:214-217.
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  • 8
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    • A second locus (GLC3B) for primary congenital glaucoma (Buphthamos) maps to the 1p36 region
    • Akarsu AN, Turacil ME, Aktan SG, et al. A second locus (GLC3B) for primary congenital glaucoma (Buphthamos) maps to the 1p36 region. Hum Mol Genet 1996;5:1199-1203.
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  • 9
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    • Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity
    • Sarfarazi M, Akarsu AN, Hossain A, et al. Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 1995; 30:171-177.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.