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Article

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia.

Haematologica - 1 Jan 2010

Lanciotti Marina, Indaco Stefania, Bonanomi Sonia, Coliva Tiziana, Mastrodicasa Elena, Caridi Gianluca, Calvillo Michaela, Dufour Carlo

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Topics

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Share to Adaptor Proteins, Signal Transducing
Share to Amino Acid Sequence
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 20065084
DOI: 10.3324/haematol.2009.015370
PMCID: PMC2805731

Genes

HAX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia.PMID 20065084Read ↗

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