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Journal Abstract Search

154 related items for PubMed ID: 9934976

  • 21.
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  • 22. Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease.
    Raskind WH, Williams CA, Hudson LD, Bird TD.
    Am J Hum Genet; 1991 Dec; 49(6):1355-60. PubMed ID: 1720927
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  • 23. PLP1 splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations.
    Bonnet-Dupeyron MN, Combes P, Santander P, Cailloux F, Boespflug-Tanguy O, Vaurs-Barrière C.
    Hum Mutat; 2008 Aug; 29(8):1028-36. PubMed ID: 18470932
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  • 25. A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesis.
    Weimbs T, Dick T, Stoffel W, Boltshauser E.
    Biol Chem Hoppe Seyler; 1990 Dec; 371(12):1175-83. PubMed ID: 1708672
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  • 32. Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice.
    Woodward K, Malcolm S.
    Trends Genet; 1999 Apr; 15(4):125-8. PubMed ID: 10203813
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  • 33. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.
    Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME.
    Am J Med Genet; 1991 Jan; 38(1):136-9. PubMed ID: 1707231
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  • 37. Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene.
    Pratt VM, Boyadjiev S, Dlouhy SR, Silver K, Der Kaloustian VM, Hodes ME.
    Am J Med Genet; 1995 Feb 13; 55(4):402-4. PubMed ID: 7539212
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  • 40. Current concepts of PLP and its role in the nervous system.
    Griffiths I, Klugmann M, Anderson T, Thomson C, Vouyiouklis D, Nave KA.
    Microsc Res Tech; 1998 Jun 01; 41(5):344-58. PubMed ID: 9672418
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