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Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome
Krumbiegel, M., Pasutto, F., Schlötzer-Schrehardt, U., Uebe, S., Zenkel, M., Mardin, C. Y., Weisschuh, N., Paoli, D., Gramer, E., Becker, C., Ekici, A. B.
, Weber, Bernhard H. F. , Nürnberg, P., Kruse, F. E. and Reis, A.
(2011)
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.
European Journal of Human Genetics 19 (2), pp. 186-193.
Date of publication of this fulltext: 11 Apr 2017 12:11
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| Item type | Article | ||||||
| Journal or Publication Title | European Journal of Human Genetics | ||||||
| Publisher: | NATURE PUBLISHING GROUP | ||||||
|---|---|---|---|---|---|---|---|
| Place of Publication: | LONDON | ||||||
| Volume: | 19 | ||||||
| Number of Issue or Book Chapter: | 2 | ||||||
| Page Range: | pp. 186-193 | ||||||
| Date | 2011 | ||||||
| Institutions | Medicine > Lehrstuhl für Humangenetik | ||||||
| Identification Number |
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| Keywords | SINGLE-NUCLEOTIDE POLYMORPHISMS; COMMON SEQUENCE VARIANTS; LOXL1 GENE POLYMORPHISMS; EXFOLIATION SYNDROME; NEUREXIN SUPERFAMILY; JAPANESE POPULATION; MYELINATED AXONS; APOLIPOPROTEIN-E; OCULAR-TISSUES; GLAUCOMA; pseudoexfoliation syndrome; DNA pooling; association study | ||||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||||
| Status | Published | ||||||
| Refereed | Yes, this version has been refereed | ||||||
| Created at the University of Regensburg | Partially | ||||||
| Item ID | 35490 |
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