Congenital Secondary Hypothyroidism Due to a Mutation C105Vfs114X Thyrotropin-β Mutation: Genetic Study of Five Unrelated Families from Switzerland and Argentina-Reference-Cited by-同舟云学术

Congenital Secondary Hypothyroidism Due to a Mutation C105Vfs114X Thyrotropin-β Mutation: Genetic Study of Five Unrelated Families from Switzerland and Argentina

Published:2003-06 Issue:6 Volume:13 Page:553-559
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Deladoëy Johnny¹,Vuissoz Jean-Marc¹,Domené Horacio M.²,Malik Naseem³,Gruneiro-Papendieck Laura²,Chiesa Ana²,Heinrich Juan J.²,Mullis Primus E.¹

Affiliation:

1. Division of Pediatric Endocrinology, University Children's Hospital, Bern, Switzerland

2. Division de Endocrinologia, Centro de Investigaciones Endocrinologicas, Hospital de Ninos "R. Gutiérrez," Buenos Aires, Argentina

3. Forensic Medicine Institute, Bern, Switzerland

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/105072503322238818

Reference23 articles.

1. Congenital Central Hypothyroidism due to a Homozygous Mutation in the Thyrotropin -Subunit Gene Follows an Autosomal Recessive Inheritance

2. Severe Congenital Hypothyroidism Due to a Homozygous Mutation of the βTSH Gene

3. Congenital Central Isolated Hypothyroidism Caused by a Homozygous Mutation in the TSH-β Subunit Gene

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