A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction-Reference-Cited by-同舟云学术

A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

Published:2003-10-15 Issue:8 Volume:112 Page:1192-1201
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Carvalho Luciani R.,Woods Kathryn S.,Mendonca Berenice B.,Marcal Nathalie,Zamparini Andrea L.,Stifani Stefano,Brickman Joshua M.,Arnhold Ivo J.P.,Dattani Mehul T.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference31 articles.

1. The development of the hypophysis cerebri of the albino rat

2. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

3. The Homeobox Gene Hesx1 Is Required in the Anterior Neural Ectoderm for Normal Forebrain Formation

4. Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

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