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Volumn 147, Issue 2, 1997, Pages 215-216

A new proteolipid lipoprotein mutation in Pelizaeus-Merzbacher disease [1]

Author keywords

[No Author keywords available]

Indexed keywords

LIPOPROTEIN; PROTEOLIPID;

EID: 0030893759     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(96)05329-4     Document Type: Letter
Times cited : (2)

References (15)
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    • (1986) , pp. 9807-9811
    • Diehl, H.-J.1    Schaich, M.2    Budzinski, R.-M.3    Stoffel, W.4
  • 3
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    • Girl with signs of Pelizæus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene
    • M.E. Hodes W.E. DeMyer V.M. Pratt M.K. Edwards S.R. Dlouhy Girl with signs of Pelizæus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene Am. J. Med. Genet. 55 1995 397 401
    • (1995) Am. J. Med. Genet. , vol.55 , pp. 397-401
    • Hodes, M.E.1    DeMyer, W.E.2    Pratt, V.M.3    Edwards, M.K.4    Dlouhy, S.R.5
  • 4
    • 0029980997 scopus 로고    scopus 로고
    • The proteolipid protein gene: double, double,…and trouble (Invited editorial) Am
    • M.E. Hodes S.R. Dlouhy The proteolipid protein gene: double, double,…and trouble (Invited editorial) Am J. Hum. Genet. 59 1996 12 15
    • (1996) J. Hum. Genet. , vol.59 , pp. 12-15
    • Hodes, M.E.1    Dlouhy, S.R.2
  • 6
    • 0024330420 scopus 로고
    • Mutation of the proteolipid protein gene PLP in a human X-chromosome linked myelin disorder
    • L.D. Hudson C. Puckett J. Berndt J. Chan S. Gencic Mutation of the proteolipid protein gene PLP in a human X-chromosome linked myelin disorder Proc. Natl. Acad. Sci. USA 86 1989 8128 8131
    • (1989) , pp. 8128-8131
    • Hudson, L.D.1    Puckett, C.2    Berndt, J.3    Chan, J.4    Gencic, S.5
  • 7
    • 0026454907 scopus 로고
    • Oculomotor and vestibular anomalies in Pelizæus Merzbacher disease: a study on a kindred with two affected and three normal males, three obligate and eight possible carriers
    • P.L.M. Huygen W.I.M. Verhagen W.O. Renier Oculomotor and vestibular anomalies in Pelizæus Merzbacher disease: a study on a kindred with two affected and three normal males, three obligate and eight possible carriers J. Neurol. Sci. 113 1992 17 25
    • (1992) J. Neurol. Sci. , vol.113 , pp. 17-25
    • Huygen, P.L.M.1    Verhagen, W.I.M.2    Renier, W.O.3
  • 11
    • 0029080845 scopus 로고
    • Pelizæus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus
    • V.M. Pratt S. Boyadjiev K. Green M.E. Hodes S.R. Dlouhy Pelizæus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus Am. J. Med. Genet. 58 1995 70 73
    • (1995) Am. J. Med. Genet. , vol.58 , pp. 70-73
    • Pratt, V.M.1    Boyadjiev, S.2    Green, K.3    Hodes, M.E.4    Dlouhy, S.R.5
  • 12
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    • (1995) Brain Pathol. , vol.5 , pp. 267-273
    • Seitelberger, F.1
  • 13
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    • Wetenswaardigheden
    • B. Smeets Wetenswaardigheden LOD-Nieuwsbrief 2 1995 18
    • (1995) LOD-Nieuwsbrief , vol.2 , pp. 18
    • Smeets, B.1
  • 14
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    • J.A. Trofatter S.R. Dlouhy W. DeMyer P.M. Conneally M.E. Hodes Pelizæus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant Proc. Natl. Acad. Sci. USA 86 1989 9427 9430
    • (1989) , pp. 9427-9430
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    • Willard, H.F.1    Riordan, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.