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Article

Neutrophil elastase mutations in congenital neutropenia.

Hematology (Amsterdam, Netherlands) - 1 Jun 2003

Ancliff Phil J, Gale Rosemary E, Linch David C

Abstract excerpt

Severe congenital neutropenia (SCN) was originally described as an autosomal recessive disorder. Autosomal dominant and sporadic forms of the disease have subsequently been recognized. All forms of the disease are manifest by persistent severe neutropenia and recurrent bacterial infection. Cyclic...

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Share to Chromosomes, Human, Pair 19
Share to Hematopoiesis
Share to Leukemia, Myeloid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukocyte Elastase

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Source

Identifiers

PMID: 12745650
DOI: 10.1080/1024533031000107497

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12745650-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Neutrophil elastase mutations in congenital neutropenia.PMID 12745650Read ↗

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