NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement-Reference-Cited by-同舟云学术

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NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

Published:2018-08-22 Issue: Volume:9 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Balicza Péter,Grosz Zoltán,Molnár Viktor,Illés Anett,Csabán Dora,Gézsi Andras,Dézsi Lívia,Zádori Dénes,Vécsei László,Molnár Mária Judit

Funder

Országos Tudományos Kutatási Alapprogramok

Magyar Tudományos Akadémia

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference14 articles.

1. Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene;Accornero;J. Clin. Endocrinol. Metab.,2010

2. Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia;Asmus;Mov. Disord.,2007

3. The requirement of Nkx2-1 in the temporal specification of cortical interneuron subtypes;Butt;Neuron,2008

4. Phenotypic insights into ADCY5-associated disease;Chang;Mov. Disord.,2016

5. TTF-1 regulates growth hormone and prolactin transcription in the anterior pituitary gland;Lee;Biochem. Biophys. Res. Commun.,2007

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Systematic review of thyroid function in NKX2-1-related disorders: Screening and diagnosis;PLOS ONE;2024-07-11

2. Differential diagnosis of Huntington’s disease− neurological aspects of NKX2-1-related disorders;Journal of Neural Transmission;2024-06-25

3. NKX2-1-conditioned disorder — «brain–lung–thyroid» syndrome: results of a multicenter study;L.O. Badalyan Neurological Journal;2024-04-27

4. Systematic review of drug therapy for chorea in NXK2‐1‐related disorders: Efficacy and safety evidence from case studies and series;European Journal of Neurology;2023-09-11

5. Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing;Frontiers in Endocrinology;2022-09-27

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