Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma

BMC Ophthalmology

Volumn 14, Issue 1, 2014, Pages

  Giardina, Emiliano ^a,b   Oddone, Francesco ^c   Lepre, Tiziana ^a   Centofanti, Marco ^c,d   Peconi, Cristina ^a   Tanga, Lucia ^c   Quaranta, Luciano ^e   Frezzotti, Paolo ^f   Novelli, Giuseppe ^a   Manni, Gianluca ^d  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

^b IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^c IRCCS FONDAZIONE BIETTI   (Italy)

^d UNIVERSITY OF ROME TOR VERGATA   (Italy)

^e UNIVERSITY OF BRESCIA   (Italy)

^f UNIVERSITY OF SIENA   (Italy)

Author keywords

Genetics; LOXL1; Pigment dispersion syndrome; Pigmentary glaucoma

Indexed keywords

LOXL1 PROTEIN, HUMAN; OXIDOREDUCTASE; RNA;

FEMALE; GENE FREQUENCY; GENETIC VARIABILITY; GENETICS; GENOTYPE; HAPLOTYPE; HUMAN; INTRAOCULAR PRESSURE; MALE; METABOLISM; MIDDLE AGED; OPEN ANGLE GLAUCOMA; PATHOPHYSIOLOGY; REAL TIME POLYMERASE CHAIN REACTION;

AMINO ACID OXIDOREDUCTASES; FEMALE; GENE FREQUENCY; GENETIC VARIATION; GENOTYPE; GLAUCOMA, OPEN-ANGLE; HAPLOTYPES; HUMANS; INTRAOCULAR PRESSURE; MALE; MIDDLE AGED; REAL-TIME POLYMERASE CHAIN REACTION; RNA;

EID: 84901436350     PISSN: None     EISSN: 14712415     Source Type: Journal    
DOI: 10.1186/1471-2415-14-52     Document Type: Article

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