Title : Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.

Pub. Date : 2018 Oct 18

PMID : 30333321






2 Functional Relationships(s)
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1 SLC26A7 is a member of the same transporter family as SLC26A4 (pendrin), an anion exchanger with affinity for iodide and chloride (among others), whose gene mutations cause congenital deafness and dyshormonogenic goiter. Chlorides solute carrier family 26, member 4 Mus musculus
2 SLC26A7 is a member of the same transporter family as SLC26A4 (pendrin), an anion exchanger with affinity for iodide and chloride (among others), whose gene mutations cause congenital deafness and dyshormonogenic goiter. Chlorides solute carrier family 26, member 4 Mus musculus