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dc.contributor.authorPJ Ojwang, RJ Pegoraro, PA Lanning, L Rom, A Motala
dc.date.accessioned2020-08-20T08:45:19Z
dc.date.available2020-08-20T08:45:19Z
dc.date.issued1999
dc.identifier.citation1en_US
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/2225
dc.descriptionThe article can be accessed in full text via URL;https://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1281037en_US
dc.description.abstractSauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS/Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS/A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRSen_US
dc.subjectNucleic acid; Diagnosis; Sibling; Genetics; Human ;Thyroid hormone;Heterozygosity; Identification Point mutationen_US
dc.subjectNegroid; Race; Target tissue resistance;Resistance ;Syndrome; Nucleotide sequence; South Africa(Republic) Africaen_US
dc.titlePoint mutation (C446S) in the thyroid hormone receptor β gene in a black South African kindred with thyroid hormone resistance syndromeen_US
dc.typeArticleen_US


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