ArticleJCI insight2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
Hakan Cangul et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
36 papers cite it
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ArticleJCI insight2018
Hakan Cangul et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.