STAC3 disorder a common cause of congenital hypotonia in Southern African patients

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dc.article.end-page23en
dc.article.start-page14en
dc.citation.doi10.1038/S41431-024-01644-5en
dc.contributor.authorFahmida Essopen
dc.contributor.authorBronwyn Dillonen
dc.contributor.authorFelicity Mhlongoen
dc.contributor.authorNtombenhle Bhenguen
dc.contributor.authorT Naickeren
dc.contributor.authorL Lambieen
dc.contributor.authorL Smiten
dc.contributor.authorK Fieggenen
dc.contributor.authorAnneline Lochanen
dc.contributor.authorJessica Dawsonen
dc.contributor.authorPhelelani Mpangaseen
dc.contributor.authorMarc Hauptfleischen
dc.contributor.authorMichael Urbanen
dc.contributor.authorE etalen
dc.contributor.authorAmanda Krauseen
dc.date.accessioned2026-04-18T20:53:00Z
dc.departmentHUMAN GENETICSen
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationSCOPUSen
dc.identifier.issn10184813en
dc.identifier.urihttps://hdl.handle.net/10539/49057
dc.journal.titleSTAC3 disorder a common cause of congenital hypotonia in Southern African patientsen
dc.journal.volume33en
dc.titleSTAC3 disorder a common cause of congenital hypotonia in Southern African patientsen
dc.typeJournal Articleen

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