Severe Tangier disease with a novel ABCA1 gene mutation.
Standard
Severe Tangier disease with a novel ABCA1 gene mutation. / Schippling, Sven; Orth, Michael; Beisiegel, Ulrike; Rosenkranz, T; Vogel, P; Münchau, Alexander; Hagel, Christian; Seedorf, U.
In: NEUROLOGY, Vol. 71, No. 18, 18, 2008, p. 1454-1455.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Harvard
Schippling, S, Orth, M, Beisiegel, U, Rosenkranz, T, Vogel, P, Münchau, A, Hagel, C & Seedorf, U 2008, 'Severe Tangier disease with a novel ABCA1 gene mutation.', NEUROLOGY, vol. 71, no. 18, 18, pp. 1454-1455. <http://www.ncbi.nlm.nih.gov/pubmed/18955690?dopt=Citation>
APA
Schippling, S., Orth, M., Beisiegel, U., Rosenkranz, T., Vogel, P., Münchau, A., Hagel, C., & Seedorf, U. (2008). Severe Tangier disease with a novel ABCA1 gene mutation. NEUROLOGY, 71(18), 1454-1455. [18]. http://www.ncbi.nlm.nih.gov/pubmed/18955690?dopt=Citation
Vancouver
Schippling S, Orth M, Beisiegel U, Rosenkranz T, Vogel P, Münchau A et al. Severe Tangier disease with a novel ABCA1 gene mutation. NEUROLOGY. 2008;71(18):1454-1455. 18.
Bibtex
@article{b64a1208fd54401184e8434060abfae9,
title = "Severe Tangier disease with a novel ABCA1 gene mutation.",
author = "Sven Schippling and Michael Orth and Ulrike Beisiegel and T Rosenkranz and P Vogel and Alexander M{\"u}nchau and Christian Hagel and U Seedorf",
year = "2008",
language = "Deutsch",
volume = "71",
pages = "1454--1455",
journal = "NEUROLOGY",
issn = "0028-3878",
publisher = "Lippincott Williams and Wilkins",
number = "18",
}
RIS
TY - JOUR
T1 - Severe Tangier disease with a novel ABCA1 gene mutation.
AU - Schippling, Sven
AU - Orth, Michael
AU - Beisiegel, Ulrike
AU - Rosenkranz, T
AU - Vogel, P
AU - Münchau, Alexander
AU - Hagel, Christian
AU - Seedorf, U
PY - 2008
Y1 - 2008
M3 - SCORING: Zeitschriftenaufsatz
VL - 71
SP - 1454
EP - 1455
JO - NEUROLOGY
JF - NEUROLOGY
SN - 0028-3878
IS - 18
M1 - 18
ER -
