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Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29

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dc.contributor.authorGEÇKİNLİ, BİLGEN BİLGE
dc.contributor.authorSÖYLEMEZ, MEHMET ALİ
dc.contributor.authorARMAN, AHMET
dc.contributor.authorsGEÇKİNLİ B. B., TÜRKYILMAZ A., ALAVANDA C., TAŞLIDERE H., SAĞER S. G., ARSLAN ATEŞ E., SÖYLEMEZ M. A., ARMAN A.
dc.date.accessioned2023-03-07T10:46:38Z
dc.date.accessioned2026-01-11T10:25:40Z
dc.date.available2023-03-07T10:46:38Z
dc.date.issued2020-06-25
dc.identifier.citationGEÇKİNLİ B. B., TÜRKYILMAZ A., ALAVANDA C., TAŞLIDERE H., SAĞER S. G., ARSLAN ATEŞ E., SÖYLEMEZ M. A., ARMAN A., \"Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29\", ESHG 2020, Avusturya, 6 - 09 Haziran 2020
dc.identifier.urihttps://www.abstractsonline.com/pp8/#!/9102/presentation/3645
dc.identifier.urihttps://hdl.handle.net/11424/287231
dc.language.isoeng
dc.relation.ispartofESHG 2020
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleRevealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29
dc.typeconferenceObject
dspace.entity.typePublication

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