Title : Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism.

Pub. Date : 2022 Jun 27

PMID : 35438852






1 Functional Relationships(s)
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1 OBJECTIVES: Iodide transport defect (ITD) is one of the principal causes of congenital hypothyroidism (CH) and its primary molecular mechanism is a mutation of the sodium/iodide symporter (NIS) gene. Sodium solute carrier family 5 member 5 Homo sapiens