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The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders. / Bech, Sara; Nørremølle, Anne; Winge, Kristian; Hasholt, Lis; Tommerup, Niels; Svenstrup, Kirsten; Nielsen, Jørgen E; Hjermind, Lena E.
I:
Parkinsonism & Related Disorders, Bind 17, Nr. 5, 01.06.2011, s. 398-9.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Bech, S
, Nørremølle, A, Winge, K
, Hasholt, L, Tommerup, N, Svenstrup, K
, Nielsen, JE & Hjermind, LE 2011, '
The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders',
Parkinsonism & Related Disorders, bind 17, nr. 5, s. 398-9.
https://doi.org/10.1016/j.parkreldis.2011.01.016APA
Bech, S.
, Nørremølle, A., Winge, K.
, Hasholt, L., Tommerup, N., Svenstrup, K.
, Nielsen, J. E., & Hjermind, L. E. (2011).
The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders.
Parkinsonism & Related Disorders,
17(5), 398-9.
https://doi.org/10.1016/j.parkreldis.2011.01.016Vancouver
Bech S
, Nørremølle A, Winge K
, Hasholt L, Tommerup N, Svenstrup K o.a.
The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders.
Parkinsonism & Related Disorders. 2011 jun. 1;17(5):398-9.
https://doi.org/10.1016/j.parkreldis.2011.01.016Author
Bech, Sara ; Nørremølle, Anne ; Winge, Kristian ; Hasholt, Lis ; Tommerup, Niels ; Svenstrup, Kirsten ; Nielsen, Jørgen E ; Hjermind, Lena E. / The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders. I: Parkinsonism & Related Disorders. 2011 ; Bind 17, Nr. 5. s. 398-9.
Bibtex
@article{f3d0dd575cd4440a8f96340cb3d1d4e1,
title = "The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders",
author = "Sara Bech and Anne N{\o}rrem{\o}lle and Kristian Winge and Lis Hasholt and Niels Tommerup and Kirsten Svenstrup and Nielsen, {J{\o}rgen E} and Hjermind, {Lena E}",
year = "2011",
month = jun,
day = "1",
doi = "10.1016/j.parkreldis.2011.01.016",
language = "English",
volume = "17",
pages = "398--9",
journal = "Parkinsonism & Related Disorders",
issn = "1353-8020",
publisher = "Elsevier",
number = "5",
}
RIS
TY - JOUR
T1 - The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders
AU - Bech, Sara
AU - Nørremølle, Anne
AU - Winge, Kristian
AU - Hasholt, Lis
AU - Tommerup, Niels
AU - Svenstrup, Kirsten
AU - Nielsen, Jørgen E
AU - Hjermind, Lena E
PY - 2011/6/1
Y1 - 2011/6/1
U2 - 10.1016/j.parkreldis.2011.01.016
DO - 10.1016/j.parkreldis.2011.01.016
M3 - Journal article
C2 - 21353620
VL - 17
SP - 398
EP - 399
JO - Parkinsonism & Related Disorders
JF - Parkinsonism & Related Disorders
SN - 1353-8020
IS - 5
ER -
