HESX1mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype
出版年份 2016 全文链接
标题
HESX1mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype
作者
关键词
-
出版物
CLINICAL ENDOCRINOLOGY
Volume 85, Issue 3, Pages 408-414
出版商
Wiley
发表日期
2016-03-22
DOI
10.1111/cen.13067
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort
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- Whole-Exome Sequencing Identifies HomozygousGPR161Mutation in a Family with Pituitary Stalk Interruption Syndrome
- (2015) Ender Karaca et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies
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- Corepressors TLE1 and TLE3 Interact with HESX1 and PROP1
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- Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development
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