BCL11B-related disease: a single phenotypic entity?

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dc.contributor.authorVedovato\\-dos\\-Santos, J. Heather
dc.contributor.authorTooze, Rebecca S.
dc.contributor.authorSithambaram, Sivagamy
dc.contributor.authorMccann, Emma
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorDogan, Ozlem A.
dc.contributor.authorKilercik, Meltem
dc.contributor.authorBingol, Aysen
dc.contributor.authorOzek, Memet M.
dc.contributor.authorJohnson, David
dc.contributor.authorNellaker, Christoffer
dc.contributor.authorWilkie, Andrew O. M.
dc.contributor.authorTwigg, Stephen R. F.
dc.date.accessioned2025-10-16T15:11:58Z
dc.date.issued2025
dc.identifier.doi10.1038/s41431-025-01824-x
dc.identifier.otherWOS:001440355600001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5158
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleBCL11B-related disease: a single phenotypic entity?
dc.typeArticle

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