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ArticleJournal of the Endocrine Society2021

Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.

Stéphanie Larrivée-Vanier et al.PubMed ↗Full text ↗Publisher ↗

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2 papers cite it

2021
2022
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Full record →Abstract, authors, funding and every citing paper · PMID 33506157