All individuals with variants in gene LRIT3

9 entries on 1 page. Showing entries 1 - 9.
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Owner     
00100098 PKRD176;61176 PubMed: Maranha 2015, Journal: Maranhao 2015, PubMed: Li 2017 - M yes Pakistan Pakistani - - - - retinal disease - 1 1 James Hejtmancik
00143966 - PubMed: Xu 2014 - M yes China Chinese - - - - retinal disease Age examination 30: first symptom: poor vision, night blindness; visual acuity OD/OS: 0,3/0,4, fundus exam.: attenuated retinal arteries, pigment deposit, no foveal reflex 1 1 Rob W.J. Collin
00246591 FamA PubMed: Zeitz 2013 2-generation family, 1 affected, unaffected heterozygous carrier father/relative F no United States - - - - - CSNB see paper; ... 2 1 Johan den Dunnen
00246592 FamB PubMed: Zeitz 2013 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F no France - - - - - CSNB see paper; ... 2 1 Johan den Dunnen
00246593 patient PubMed: Zeitz 2015, Journal: Zeitz 2015 - - - United States - - - - - CSNB see paper; ... 1 1 Johan den Dunnen
00293516 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 16 Mohammed Faruq
00304973 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00358872 patient PubMed: Dan 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F no China - - - - - CSNB see paper; ..., Schubert-Bornschein congenital stationary night blindness 2 1 Johan den Dunnen
00375405 - PubMed: Zeitz 2015 - - - United States - - - - - retinal disease see paper; ... 1 1 LOVD
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