Familial isolated growth hormone deficiency: genetics and pathophysiology

Endocr J. 2002 Jun;49(3):265-72. doi: 10.1507/endocrj.49.265.

Authors

Yoshsitaka Hayashi¹, Takashi Kamijo, Masamichi Ogawa, Hisao Seo

Affiliation

¹ Department of Endocrinology and Metabolism, Research Institute of Environmental Medicine, Nagoya University, Nagoya 464-8601, Japan.

PMID: 12201208
DOI: 10.1507/endocrj.49.265

No abstract available

Publication types

Review

MeSH terms

Base Sequence / genetics
Chromosomes, Human, X
Genes, Dominant
Genes, Recessive
Genetic Linkage
Human Growth Hormone / deficiency*
Humans
Metabolism, Inborn Errors / classification
Metabolism, Inborn Errors / genetics*
Metabolism, Inborn Errors / physiopathology*
Molecular Sequence Data
Receptors, Neuropeptide / genetics
Receptors, Pituitary Hormone-Regulating Hormone / genetics

Substances

Receptors, Neuropeptide
Receptors, Pituitary Hormone-Regulating Hormone
Human Growth Hormone
somatotropin releasing hormone receptor