All individuals with variants in gene INF2

7 entries on 1 page. Showing entries 1 - 7.
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AscendingIndividual ID     

ID_report     

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VIP     

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Owner     
00018450 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - ? - 1 1 Elisabet Ars Criach
00018844 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - ? - 1 1 Elisabet Ars Criach
00208809 - - - F - Germany - - - - - - HP:0001761 (Pes cavus); HP:0003401 (Paresthesia) 1 1 Andreas Laner
00218998 28902413-Pat8 PubMed: Dohrn 2017, Journal: Dohrn 2017 analysis 612 patients F - (Germany) - - - - - CMT CMT-DIE; no family history; typical phenotype with CMT and focal segmental glomerulosclerosis 1 1 Johan den Dunnen
00301048 - PubMed: Büscher 2018 4-generation family, 14 affected (6F, 8M) M no Germany - 44y - - - FSGS5 - 1 7 Matthias Braunisch
00414390 WHP57 PubMed: Sun 2018 - M - China - - - - - ? Focal Segmental Glomerulosclerosis 5; Alport Syndrome; Hemolytic Uremic syndrome susceptibility to 1 1 1 LOVD
00414480 WHP147 PubMed: Sun 2018 - F - China - - - - - ? Cystinuria;Focal Segmental Glomerulosclerosis 5 1 1 LOVD
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