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Article

Frequent Constitutional C to T Mutations in CGA-Arginine Codons in the RB1 Gene Produce Premature Stop Codons in Patients with Bilateral (Hereditary) Retinoblastoma

1 Jan 1994

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

Identifiers

PMID: 7704558
DOI: 10.1159/000472372

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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.

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Frequent Constitutional C to T Mutations in CGA-Arginine Codons in the RB1 Gene Produce Premature Stop Codons in Patients with Bilateral (Hereditary) RetinoblastomaPMID 7704558Read ↗

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Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysis.Semantic proximity Read ↗

Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.Semantic proximity Read ↗

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High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons.Semantic proximity Read ↗

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