Eps8l2 is new causal gene for childhood onset autosomal recessive progressive hearing loss

HIGHLIGHTS

• who: Malika Dahmani et al. from the (UNIVERSITY) have published the research: EPS8L2 is new causal gene for childhood onset autosomal recessive progressive hearing loss, in the Journal: (JOURNAL)
• what: The authors report the study of two Algerian siblings born to consanguineous parents, and affected by progressive hearing loss. The authors report the identification, by whole-exome sequencing (WES), of a new causal gene for recessively inherited progressive deafness in an Algerian family.

SUMMARY

Whole-exome sequencing allowed the authors to identify a new gene responsible for childhood progressive hearing loss . . .

 



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