Title : Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.

Pub. Date : 2022

PMID : 35600585






1 Functional Relationships(s)
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1 ITD is an autosomal recessive disorder caused by loss-of-function variants in the sodium/iodide symporter (NIS)-coding SLC5A5 gene. Sodium solute carrier family 5 member 5 Homo sapiens