A Novel NKX2.1 Mutation in a Family with Hypothyroidism and Benign Hereditary Chorea
Author:
Affiliation:
1. Dipartimento di Endocrinologia ed Oncologia Molecolare e Clinica, Università degli Studi di Napoli “Federico II,” Napoli, Italy.
2. Dipartimento di Scienze Neurologiche, Università degli Studi di Napoli “Federico II,” Napoli, Italy.
Publisher
Mary Ann Liebert Inc
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.liebertpub.com/doi/pdf/10.1089/thy.2008.0085
Reference27 articles.
1. Thyroid Development and Its Disorders: Genetics and Molecular Mechanisms
2. A Population-Based Study on the Frequency of Additional Congenital Malformations in Infants with Congenital Hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism (1991-1998)
3. Benign hereditary chorea Clinical and genetic aspects
4. Clinical and genetic heterogeneity in benign hereditary chorea
5. The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary.
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