Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

Peter P. Pramstaller; Bernhard Kis; Cordula Eskelson; Katja Hedrich; Monika Scherer; Eberhard Schwinger; Xandra O. Breakefield; Patricia L. Kramer; Laurie J. Ozelius; Christine Klein

doi:10.1002/mds.10071

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

Peter P. Pramstaller, Bernhard Kis, Cordula Eskelson, Katja Hedrich, Monika Scherer, Eberhard Schwinger, Xandra O. Breakefield, Patricia L. Kramer, Laurie J. Ozelius, Christine Klein

Neurology

Research output: Contribution to journal › Article › peer-review

22 Scopus citations

Original language	English (US)
Pages (from-to)	424-426
Number of pages	3
Journal	Movement Disorders
Volume	17
Issue number	2
DOIs	https://doi.org/10.1002/mds.10071
State	Published - Mar 2002

ASJC Scopus subject areas

Neurology
Clinical Neurology

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10.1002/mds.10071

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@article{6409ad40b32b4e46a51e5975bba1585f,

title = "Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene",

author = "Pramstaller, {Peter P.} and Bernhard Kis and Cordula Eskelson and Katja Hedrich and Monika Scherer and Eberhard Schwinger and Breakefield, {Xandra O.} and Kramer, {Patricia L.} and Ozelius, {Laurie J.} and Christine Klein",

year = "2002",

month = mar,

doi = "10.1002/mds.10071",

language = "English (US)",

volume = "17",

pages = "424--426",

journal = "Movement Disorders",

issn = "0885-3185",

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T1 - Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

AU - Pramstaller, Peter P.

AU - Kis, Bernhard

AU - Eskelson, Cordula

AU - Hedrich, Katja

AU - Scherer, Monika

AU - Schwinger, Eberhard

AU - Breakefield, Xandra O.

AU - Kramer, Patricia L.

AU - Ozelius, Laurie J.

AU - Klein, Christine

PY - 2002/3

Y1 - 2002/3

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DO - 10.1002/mds.10071

M3 - Article

C2 - 11921141

AN - SCOPUS:0036523867

SN - 0885-3185

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SP - 424

EP - 426

JO - Movement Disorders

JF - Movement Disorders

IS - 2

ER -

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

ASJC Scopus subject areas

Access to Document

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