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 Malaysia

负责人：

关键词：

Paediatric clinical genetics & dysmorphology;Thyroid disease;Paediatric endocrinology;Molecular Biology

DOI：

doi:10.5061/dryad.5230v

摘要：

. Participants: Twelve biologically unrelated Malaysian-Chinese patients with congenital hypothyroidism were recruited in this study. All patients showed high TSH