Research Project:
From Mendelian Diseases to Functional Genomics for Therapeutic Innovation

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dc.contributor.departmentSchool of Medicine
dc.contributor.departmentSchool of Medicine
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-12-29T10:39:24Z
dc.date.available2024-12-29
dc.description.publisherscopeNational
dc.identifierTB.00518
dc.identifier.urihttps://hdl.handle.net/20.500.14288/24766
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Projects Collection
dc.relation.relatedpublicationsRAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis
dc.relation.relatedpublicationsA progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencing
dc.titleFrom Mendelian Diseases to Functional Genomics for Therapeutic Innovation
dc.title.alternativeFrom Mendelian Diseases to Functional
dspace.entity.typeProject
local.contributor.kuauthorBeillard, Nathalie Sonia Escande
local.project.contractnumber118C318
local.project.endDate2024-06-01
local.project.startDate2020-08-31
local.project.templateTB.BIDEB.2232
project.funder.identifierTÜBİTAK
project.funder.nameTÜBİTAK
project.investigatorBeillard, Nathalie Sonia Escande
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