Data from: The prevalence of c.2268dup and detection of two novel alterations, c.670_672del and c.1186C>T, in the TPO gene in a cohort of Malaysian-Chinese with thyroid dyshormonogenesis

Objectives: The c.2268dup mutation in the thyroid peroxidase (TPO) gene is the most common TPO alteration reported in Taiwanese patients with thyroid dyshormonogenesis. The ancestors of these patients are believed to originate from the southern province of China. Our previous study showed that this...

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Bibliographische Detailangaben

Hauptverfasser:	Lee, Ching Chin, Harun, Fatimah, Jalaludin, Muhammad Yazid, Heh, Choon Han, Othman, Rozana, Mat Junit, Sarni
Format:	Dataset
Sprache:	eng
Schlagworte:	Molecular biology Paediatric clinical genetics & dysmorphology Paediatric endocrinology Thyroid disease
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