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Article

Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation.

Gene - 1 Dec 2012

Mosrati Mohamed Ali, Schrauwen Isabelle, Kamoun Hassen, Charfeddine Ilhem, Fransen Erik, Ghorbel Abdelmonem, Van Camp Guy, Masmoudi Saber

Abstract excerpt

Hearing loss is a common congenital anomaly with an incidence of 1 in 1000 live births. It has been described together with several other clinical features as fortuitous association or commune genetic syndrome. In this study, we investigated a consanguineous Tunisian family with moderate to profo...

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Identifiers

PMID: 22975208
DOI: 10.1016/j.gene.2012.09.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22975208-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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