All individuals with variants in gene NDUFA3

6 entries on 1 page. Showing entries 1 - 6.
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VIP     

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Owner     
00382950 iw237 - mitochondrial complex I deficiency M no China Chinese - - - - ? HP:0004325; HP:0000364; HP:0001263; HP:0002317 2 1 Wenjuan Qiu
00385847 22 PubMed: Cho 2020 - M - (United States) - - - - - retinal disease - 1 1 LOVD
00426363 RP-0777_III:1 PubMed: Martin-Merida 2017 family RP-0777, individual III:1, proband M - Spain Spanish - - - - retinal disease symptoms (age, years): night blindness: 27; visual field constriction: 32; visual acuity loss: no; best corrected visual acuity right/left eye: ; visual field: islands; electroretinogram: ; fundus aspect: 1 1 LOVD
00426364 RP-0777_II:4 PubMed: Martin-Merida 2017 family RP-0777, individual II:4, proband's father M - Spain Spanish - - - - retinal disease - 1 1 LOVD
00426367 RP-0932_III:12 PubMed: Martin-Merida 2017 family RP-0932, individual III:12, proband's father's paternal cousin F - Spain Spanish - - - - retinal disease symptoms (age, years): night blindness: unknown; visual field constriction: 14; visual acuity loss: 13; best corrected visual acuity right/left eye: 0.7/0.8; visual field: tubular; electroretinogram: nonrecordable; fundus aspect: typical rp; additional findings: none 1 1 LOVD
00426368 RP-0932_IV:12 PubMed: Martin-Merida 2017 family RP-0932, individual IV:12, proband's father's paternal cousin's daughter F - Spain Spanish - - - - retinal disease symptoms (age, years): night blindness: unknown; visual field constriction: 17; visual acuity loss: no; best corrected visual acuity right/left eye: not available; visual field: not available; electroretinogram: not available; fundus aspect: not available; additional findings: none 1 1 LOVD
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