All individuals with variants in gene C12orf65

12 entries on 1 page. Showing entries 1 - 12.
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00080916 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COXPD7 Combined oxidative phosphorylation deficiency 7 (OMIM:613559) 1 1 Daniel Trujillano
00150170 26539891-FamBAB4635 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? Hypergonadotrophic hypogonadism, corpus callosum hypoplasia 1 2 Johan den Dunnen
00204610 - - - M - - Dutch - - - - LS - 1 1 LOVD
00204611 - - Both parents (and an older sister) were heterozygous carriers of the mutation, making it unlikely. An older brother was homozygous for the wild-type allele. F - - Turkish - - - - LS - 1 1 LOVD
00204612 - - Father of Pat1 M - - Turkish - - - - Healthy/Control - 1 1 LOVD
00204613 - - Mother of Pat1 F - - Turkish - - - - Healthy/Control - 1 1 LOVD
00204614 - - Sister of Pat1 F - - Turkish - - - - Healthy/Control - 1 1 LOVD
00290629 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 21 Mohammed Faruq
00296588 Pat21 PubMed: Taylor 2014 2 affected F - Ireland Irish - - - - ? muscle affected; central nervous system affected; heart not affected; liver not affected; lactic acidosis, optic atrophy, mtDNA depletion 1 2 Johan den Dunnen
00374227 S-3353 PubMed: Ganapathy 2019 - - - India - - - - - ? Visual disturbance, frequent falls, progressive gait difficulty, oculomotor apraxia, spasticity, cognitive deficit and peripheral neuropathy 1 1 Johan den Dunnen
00390468 G013375 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - NDD - 1 1 LOVD
00461160 F019P020II-2 PubMed: Zheng 2024 - M - China - - - - - OPA see paper; ..., congenital; best corrected visual acuity (first visit) OD 0.05/OS 0.1; fundus oculi (first visit) OD temporal pallor, ARV/OS temporal pallor, ARV; electrophysiology moderately reduced (rod/cone); bilateral nystagmus; 2 1 Johan den Dunnen
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