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    Results: 4

    1.

    Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.

    Finsterer J, Löscher W, Quasthoff S, Wanschitz J, Auer-Grumbach M, Stevanin G.

    J Neurol Sci. 2012 Jul 15;318(1-2):1-18. doi: 10.1016/j.jns.2012.03.025. Epub 2012 May 1. Review.

    PMID:
    22554690
    [PubMed - indexed for MEDLINE]
    2.

    Pelizaeus-Merzbacher disease, Pelizaeus-Merzbacher-like disease 1, and related hypomyelinating disorders.

    Hobson GM, Garbern JY.

    Semin Neurol. 2012 Feb;32(1):62-7. doi: 10.1055/s-0032-1306388. Epub 2012 Mar 15. Review.

    PMID:
    22422208
    [PubMed - indexed for MEDLINE]
    3.

    A novel PLP1 mutation further expands the clinical heterogeneity at the locus.

    Hand CK, Bernard G, Dubé MP, Shevell MI, Rouleau GA.

    Can J Neurol Sci. 2012 Mar;39(2):220-4.

    PMID:
    22343157
    [PubMed - indexed for MEDLINE]
    4.

    An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene.

    Suzuki SO, Iwaki T, Arakawa K, Furuya H, Fujii N, Iwaki A.

    Acta Neuropathol. 2011 Dec;122(6):775-81. doi: 10.1007/s00401-011-0916-x. Epub 2011 Nov 20.

    PMID:
    22101368
    [PubMed - indexed for MEDLINE]

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