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Article

A Case Study on PPM1D and 9 Other Shared Germline Alterations in a Family.

Asian Pacific journal of cancer prevention : APJCP - 1 Jun 2023

Biswas Shristi, Manekar Swati, Bakshi Sonal Rajiv

Abstract excerpt

BACKGROUND: The use of high-throughput genotyping techniques has enabled us to identify the rare germline genetic variants with different pathogenicity and penetrance, and understand their role in cancer predisposition. We report here a familial cancer case, a study from Western Indian. METHODS: NGS-WES was carried out in a lung cancer patient who has a family history of multiple cancers across generations,...

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Identifiers

PMID: 37378944
DOI: 10.31557/APJCP.2023.24.6.2129
PMCID: PMC10505862

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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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