Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
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| Description | scientific article published on 18 October 2018 |
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author: Carl A Anderson Fiona E Karet Frankl Erdal Eren Jarmo Jääskeläinen Eamonn R Maher Christoffer Löf Timothy Barrett Jukka Kero |
| Publication date | October 18, 2018 |
| Language | English |
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