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Article

De novo SOX10 nonsense mutation in a patient with Kallmann syndrome and hearing loss.

Pediatric research - 1 Jul 2014

Vaaralahti Kirsi, Tommiska Johanna, Tillmann Vallo, Liivak Natalja, Känsäkoski Johanna, Laitinen Eeva-Maria, Raivio Taneli

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24769923
DOI: 10.1038/pr.2014.60

Genes

SOX10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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