Identification of a novel somatic mutation of POU6F2 by whole‐genome sequencing in prolactinoma
Author:
Affiliation:
1. Department of Cell Biology Beijing Neurosurgical Institute Capital Medical University Beijing China
2. Department of Neurosurgery Beijing Tiantan Hospital Affiliated to Capital Medical University Beijing China
Funder
National Natural Science Foundation of China
Beijing Nova Program
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1022
Reference22 articles.
1. Novel Genetic Causes of Pituitary Adenomas
2. Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients
3. AIPMutation in Pituitary Adenomas in the 18th Century and Today
4. A dominant variant in DMXL2 is linked to nonsyndromic hearing loss
5. The Murine Pou6f2 Gene is Temporally and Spatially Regulated During Kidney Embryogenesis and its Human Homolog is Overexpressed in a Subset of Wilms Tumors
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