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TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews.
Shaki, David; Eskin-Schwartz, Marina; Hadar, Noam; Bosin, Emily; Carmon, Lior; Refetoff, Samuel; Hershkovitz, Eli; Birk, Ohad S; Haim, Alon.
Afiliação
  • Shaki D; Pediatric Endocrinology Unit, Saban Pediatric Medical Center for Israel, Beer Sheva, Israel.
  • Eskin-Schwartz M; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Hadar N; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Bosin E; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Carmon L; Endocrinology Lab, Soroka University Medical Center, Beer Sheva, Israel.
  • Refetoff S; Pediatric Endocrinology Unit, Saban Pediatric Medical Center for Israel, Beer Sheva, Israel.
  • Hershkovitz E; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Birk OS; Departments of Medicine and Pediatrics and the Committee on Genetics, The University of Chicago, Chicago, Illinois, USA.
  • Haim A; Pediatric Endocrinology Unit, Saban Pediatric Medical Center for Israel, Beer Sheva, Israel.
Eur Thyroid J ; 11(1)2022 01 07.
Article em En | MEDLINE | ID: mdl-34981755
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article