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. 2021 Nov 9;246(21):NP5. doi: 10.1177/15353702211040362

Corrigendum to A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

PMCID: PMC8581821  PMID: 34749523

Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin K Esoh, Thashi Bharadwaj, Liz M Nouel-Saied, Anushree Acharya, Abdul Nasir, Suzanne M Leal, Ambroise Wonkam. A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. Exp Biol Med (Maywood), 2021 July;246 (13):1524–1532, doi:10.1177/1535370221999746

In this article the title was incorrect. The correct title is shown below.

A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.

The article has been corrected.


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