Nicotinamide nucleotide transhydrogenase mutation analysis in Chinese patients with thyroid dysgenesis-Reference-Cited by-同舟云学术

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Nicotinamide nucleotide transhydrogenase mutation analysis in Chinese patients with thyroid dysgenesis

Published:2021-09-21 Issue:1 Volume:188 Page:89-98
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Li Miaomiao¹^ORCID,Tian Weibing²,Wang Fengqi¹,Yang Chengyu¹,Zhang Lu¹,Tang Qian¹,Liu Shiguo¹,Wang Fang³

Affiliation:

1. The Affiliated Hospital of Qingdao University Medical Genetic Department, Prenatal Diagnosis Center Qingdao China

2. Weifang Maternal and Child Health Hospital Newborn Screening Center Weifang China

3. The Affiliated Hospital of Qingdao University Department of Endocrinology Qingdao China

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62493

Reference39 articles.

1. Disorders of thyroid morphogenesis

2. Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction

3. Mutations in BOREALIN cause thyroid dysgenesis;Carré A.;Human Molecular Genetics,2017

4. Spectrum of Human Foxe1/TTF2 Mutations

5. Nicotinamide Nucleotide Transhydrogenase as a Novel Treatment Target in Adrenocortical Carcinoma

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2. Lack of NAD(P)+ transhydrogenase activity in patients with primary adrenal insufficiency due to NNT variants;European Journal of Endocrinology;2024-01-23

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