Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss - Concepedia

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Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss

DOI Full Paper Access

22

Citations

5

References

2014

Year

Érika L. Freitas, Jeanne Oiticica, Amanda G Silva, Roseli Saraiva Moreira Bittar, Carla Rosenberg, Regina Célia Mingroni‐Netto

European Journal of Medical Genetics

Mendelian DisorderGenetic DisorderGeneticsAudiologyPathologyEntire Pou4f3 GeneDisease Gene IdentificationCochlear DevelopmentHuman HearingArtsMedicineFamilial CaseHearing Loss

References

	Year	Citations

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