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Article

A homozygous kinase-defective mutation in the insulin receptor gene in a patient with leprechaunism

20 Mar 1997

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Share to Growth Hormone and Insulin-like Growth Factors
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Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 9112018
DOI: 10.1007/s001250050695

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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A homozygous kinase-defective mutation in the insulin receptor gene in a patient with leprechaunismPMID 9112018Read ↗

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Deletion of 3 basepairs resulting in the loss of lysine-121 in the insulin receptor alpha-subunit in a patient with leprechaunism: binding, phosphorylation, and biological activity.Semantic proximity Read ↗

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Mutations in the insulin receptor gene.Semantic proximity Read ↗

Identification and functional assessment of novel and known insulin receptor mutations in five patients with syndromes of severe insulin resistance.Semantic proximity Read ↗

[Leprechaunism caused by mutations in the insulin receptor gene].Semantic proximity Read ↗

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Amplification and analysis of promoter region of insulin receptor gene in a patient with leprechaunism associated with severe insulin resistance.Semantic proximity Read ↗

Genotype-phenotype correlation in inherited severe insulin resistance.Semantic proximity Read ↗

Leprechaunism (Donohue syndrome): a case bearing novel compound heterozygous mutations in the insulin receptor gene.Semantic proximity Read ↗

[Mutations in the insulin receptor gene].Semantic proximity Read ↗

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