All individuals with variants in gene KIF3B

6 entries on 1 page. Showing entries 1 - 6.
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00301199 FamAPatII1 PubMed: Cogné 2020 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - ? retinitis pigmentosa, hepatic fibrosis, postaxial hexadactyly both hands and right foot, bicuspid aortic valve, normal kidney 1 1 Johan den Dunnen
00301200 FamBPatIV1 PubMed: Cogné 2020 6-generation family, 19 affected 10(F, 9M) M - United States Jewish-Ashkenazi - - - - retinal disease retinitis pigmentosa, visual field 10;10, no hepatic fibrosis, no skeletal malformations, normal heart, normal kidney 1 19 Johan den Dunnen
00301201 FamBPatIV3 PubMed: Cogné 2020 - M - United States Jewish-Ashkenazi - - - - retinal disease retinitis pigmentosa, visual field 20;22, no hepatic fibrosis, no skeletal malformations, normal heart, normal kidney 1 1 Johan den Dunnen
00301202 FamBPatV4 PubMed: Cogné 2020 - F - United States Jewish-Ashkenazi - - - - retinal disease retinitis pigmentosa, no hepatic fibrosis, no skeletal malformations (postaxial hexadacty mother/brother), normal heart, normal kidney 1 1 Johan den Dunnen
00301203 FamBPatVI2 PubMed: Cogné 2020 - F - United States Jewish-Ashkenazi - - - - retinal disease retinitis pigmentosa, visual field 20UU, no hepatic fibrosis, no skeletal malformations, normal heart, normal kidney 1 1 Johan den Dunnen
00301204 FamBPatIVI1 PubMed: Cogné 2020 - M - United States Jewish-Ashkenazi - - - - retinal disease retinitis pigmentosa, constricted central vision, severe symptoms, no hepatic fibrosis, no skeletal malformations, normal heart, kidney issues (dialysis) 1 1 Johan den Dunnen
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