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

Research output: Contribution to journalArticle

20 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)424-426
Number of pages3
JournalMovement Disorders
Volume17
Issue number2
DOIs
StatePublished - Mar 2002

Fingerprint

Chromosome Deletion
Ubiquitin-Protein Ligases
Neurologic Examination
Pedigree
Ligases
Parkinson Disease
Phenotype
Genes

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

Cite this

Pramstaller, P. P., Kis, B., Eskelson, C., Hedrich, K., Scherer, M., Schwinger, E., ... Klein, C. (2002). Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene. Movement Disorders, 17(2), 424-426. https://doi.org/10.1002/mds.10071

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene. / Pramstaller, Peter P.; Kis, Bernhard; Eskelson, Cordula; Hedrich, Katja; Scherer, Monika; Schwinger, Eberhard; Breakefield, Xandra O.; Kramer, Patricia L.; Ozelius, Laurie J.; Klein, Christine.

In: Movement Disorders, Vol. 17, No. 2, 03.2002, p. 424-426.

Research output: Contribution to journalArticle

Pramstaller, PP, Kis, B, Eskelson, C, Hedrich, K, Scherer, M, Schwinger, E, Breakefield, XO, Kramer, PL, Ozelius, LJ & Klein, C 2002, 'Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene', Movement Disorders, vol. 17, no. 2, pp. 424-426. https://doi.org/10.1002/mds.10071
Pramstaller PP, Kis B, Eskelson C, Hedrich K, Scherer M, Schwinger E et al. Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene. Movement Disorders. 2002 Mar;17(2):424-426. https://doi.org/10.1002/mds.10071
Pramstaller, Peter P. ; Kis, Bernhard ; Eskelson, Cordula ; Hedrich, Katja ; Scherer, Monika ; Schwinger, Eberhard ; Breakefield, Xandra O. ; Kramer, Patricia L. ; Ozelius, Laurie J. ; Klein, Christine. / Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene. In: Movement Disorders. 2002 ; Vol. 17, No. 2. pp. 424-426.
@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 = "3",
doi = "10.1002/mds.10071",
language = "English (US)",
volume = "17",
pages = "424--426",
journal = "Movement Disorders",
issn = "0885-3185",
publisher = "John Wiley and Sons Inc.",
number = "2",

}

TY - JOUR

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

UR - http://www.scopus.com/inward/record.url?scp=0036523867&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0036523867&partnerID=8YFLogxK

U2 - 10.1002/mds.10071

DO - 10.1002/mds.10071

M3 - Article

VL - 17

SP - 424

EP - 426

JO - Movement Disorders

JF - Movement Disorders

SN - 0885-3185

IS - 2

ER -