All individuals with variants in gene RAB28

19 entries on 1 page. Showing entries 1 - 19.
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00155527 - Sharon, submitted - F yes Israel Morocco;Jewish - - - - LCA - 1 2 Dror Sharon
00309330 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309613 FamA PubMed: Roosing 2013 2-generation family, 3 affected 2(F, M), unaffected parents - - Germany - - - - - retinal disease see paper; ... 1 3 Johan den Dunnen
00309614 FamB PubMed: Roosing 2013 2-generation family, 2 affected (F, M), unaffected heterozygous carrier parents - yes Morocco Jewish - - - - retinal disease see paper; ... 1 2 Johan den Dunnen
00309615 MD-0312 PubMed: Riveiro-Alvarez 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Spain - - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00309616 MD-0448 PubMed: Riveiro-Alvarez 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Spain - - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00309617 patient PubMed: Lee 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Korea - - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00309618 family PubMed: Jespersgaard 2020 4-generation family, 2 affected (2M), unaffected heterozygous carrier parents M - Denmark - - - - - retinal disease see paper; ... 1 2 Johan den Dunnen
00362922 CHRO249 PubMed: Weisschuh 2016 family - - Germany - - - - - retinal disease see paper; ... 1 1 LOVD
00375430 RP#024 PubMed: Katagiri 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00379750 IR_GH_0094 - - F - Korea, South (Republic) - - - - - CORD HP:0000662, HP:0000613, HP:0001123, HP:0000551, HP:0000548 1 1 Jinu Han
00379758 IR_GH_0104 - - M - Korea, South (Republic) - - - - - CORD HP:0030515, HP:0000613, HP:0001129, HP:0000551, HP:0000548 1 1 Jinu Han
00382590 452 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 1 1 LOVD
00386247 RPN-482 PubMed: Rodriguez-Munoz 2020 family fRPN-214, proband M - Spain - - - - - retinal disease - 1 1 LOVD
00447003 ARRP-460 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00447543 CRD-838 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00450967 072206 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450968 072241 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - M - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450969 080604 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
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