Analysis of CNTNAP2 polymorphisms in Polish population with pseudoexfoliation syndrome

Acta Ophthalmologica

Volumn 90, Issue 8, 2012, Pages

  Malukiewicz, Grazyna ^a   Lesiewska Junk, Hanna ^a,c   Linkowska, Katarzyna ^b   Grzybowski, Tomasz ^b   Kaźmierczak, Karolina ^a  

^a NICOLAUS COPERNICUS UNIVERSITY   (Poland)

^b NICOLAUS COPERNICUS UNIVERSITY   (Poland)

^c NONE   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

AGED; CLINICAL ARTICLE; CONTACTIN ASSOCIATED PROTEIN LIKE 2 GENE; CONTROLLED STUDY; DNA SEQUENCE; ETHNIC GROUP; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HUMAN; LETTER; MALE; MOLECULAR PATHOLOGY; POLISH; POPULATION RESEARCH; PRIORITY JOURNAL; PSEUDOEXFOLIATION; SINGLE NUCLEOTIDE POLYMORPHISM;

AGED; ALLELES; EXFOLIATION SYNDROME; FEMALE; HAPLOTYPES; HUMANS; MALE; MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; POLAND; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84870522199     PISSN: 1755375X     EISSN: 17553768     Source Type: Journal    
DOI: 10.1111/j.1755-3768.2012.02395.x     Document Type: Letter

References (5)

1. Arnarsson AM, (2009): Epidemiology of exfoliation syndrome in the Reykjavik Eye Study. Acta Ophthalmol 87: 1-17.
2. Challa P, Schmidt S, Liu Y, Qin X, Vann RR, Gonzalez P, Allingham RR, &, Hauser MA, (2008): Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma. Mol Vis 14: 146-149.
3. Kayser M, Lao O, Anslinger K, et al., (2005): Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis. Hum Genet 117: 428-443.
4. Krumbiegel M, Pasutto F, Schlotzer-Schrehardt U, et al., (2011): Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. Eur J Hum Genet 19: 186-193.
5. Malukiewicz G, Lesiewska-Junk H, Linkowska K, Mielnik M, Grzybowski T, &, Sulima N, (2011): Analysis of LOXL1 single nucleotide polymorphisms in Polish population with pseudoexfoliation syndrome. Acta Ophthalmol 89: 64-66.