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Article

Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 gene.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Oct 2013

Awano Hiroyuki, Lee Tomoko, Yagi Mariko, Masamune Atsushi, Kume Kiyoshi, Takeshima Yasuhiro, Iijima Kazumoto

Abstract excerpt

Hereditary pancreatitis (HP) is an autosomal-dominant gene disorder. The affected genes have been identified as the cationic trypsinogen (CT) gene and the serine protease inhibitor Kazal type 1 (SPINK1) gene. These gene abnormalities alone, however, do not necessarily regulate the onset or severi...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24134754
DOI: 10.1111/ped.12152

Genes

SPINK1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-24134754-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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