Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism-Reference-Cited by-同舟云学术

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Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism

Published:2012-09-24 Issue:9 Volume:7 Page:e46008
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Takagi Masaki,Ishii Tomohiro,Inokuchi Mikako,Amano Naoko,Narumi Satoshi,Asakura Yumi,Muroya Koji,Hasegawa Yukihiro,Adachi Masanori,Hasegawa Tomonobu

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Cited by 23 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. Genetic Profiles and Three-year Follow-up Study of Chinese Males With Congenital Hypogonadotropic Hypogonadism;The Journal of Sexual Medicine;2021-09

2. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome;Frontiers in Pediatrics;2021-02-02

3. Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort;Clinical Endocrinology;2020-12-21

4. Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity;Pituitary;2020-09-07

5. Development of the Pituitary Gland;Comprehensive Physiology;2020-03-12

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