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

Mutations in transcription factors genes, which are well regulated spatially and temporally in the pituitary gland, result in congenital hypopituitarism (CH) in humans. The prevalence of CH attributable to transcription factor mutations appears to be rare and varies among populations. This study aim...

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Detalhes bibliográficos
Main Authors: Takagi, Masaki, Ishii, Tomohiro, Inokuchi, Mikako, Amano, Naoko, Narumi, Satoshi, Asakura, Yumi, Muroya, Koji, Hasegawa, Yukihiro, Adachi, Masanori, Hasegawa, Tomonobu
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3454328/
https://ncbi.nlm.nih.gov/pubmed/23029363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0046008
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