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

^*Corresponding author for this work

Institute of Neurogenetics

23 Citations (Scopus)

Original language	English
Journal	Movement Disorders
Volume	17
Issue number	2
Pages (from-to)	424-426
Number of pages	3
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.10071
Publication status	Published - 01.03.2002

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10.1002/mds.10071

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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",

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doi = "10.1002/mds.10071",

language = "English",

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 - 2002/3/1

Y1 - 2002/3/1

UR - https://www.scopus.com/pages/publications/0036523867

U2 - 10.1002/mds.10071

DO - 10.1002/mds.10071

M3 - Journal articles

C2 - 11921141

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SN - 0885-3185

VL - 17

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

UN SDGs

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