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Article

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance.

The Journal of clinical endocrinology and metabolism - 1 Sept 2003

Germain-Lee Emily L, Groman Joshua, Crane Janet L, Jan de Beur Suzanne M, Levine Michael A

Abstract excerpt

Albright hereditary osteodystrophy (AHO) is a genetic disorder caused by heterozygous inactivating mutations in GNAS1, the gene encoding the alpha-chain of G(s), and is associated with short stature, obesity, brachydactyly, and sc ossifications. AHO patients with GNAS1 mutations on maternally inh...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to GTP-Binding Protein alpha Subunits, Gs

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Source

Identifiers

PMID: 12970262
DOI: 10.1210/jc.2003-030028

Genes

GHRH
PTH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12970262-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance.PMID 12970262Read ↗

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