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Pasutto F 2

Showing records 1 to 2 | Display all abstracts from Pasutto F

46763 Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open angle glaucoma
Pasutto F; Matsumoto T; Mardin CY; Sticht H; Brandstatter JH; Michels-Rautenstrauss K; Weisschuh N; Gramer E; Ramdas WD; van Koolwijk LME
Medizinische Genetik 2010; 22: 87

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46764 Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome and pseu-doexfoliation glaucoma
Krumbiegel M; Pasutto F; Schlotzer-Schrehardt U; Uebe S; Zenkel M; Mardin CY; Weisschuh N; Paoli D; Gramer E; Becker C
Medizinische Genetik 2010; 22: 131

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