Corrigendum to A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family
- PMID: 34749523
- PMCID: PMC8581821
- 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
Erratum for
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A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.Exp Biol Med (Maywood). 2021 Jul;246(13):1524-1532. doi: 10.1177/1535370221999746. Epub 2021 Mar 9. Exp Biol Med (Maywood). 2021. PMID: 33715530 Free PMC article.
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