A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss - Concepedia

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A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

DOI Full Paper Access

72

Citations

22

References

2010

Year

Aslı Sırmacı, Seyra Erbek, Justin Price, Mingqian Huang, Duygu Duman, Filiz Başak Cengiz, Güney Bademci, Suna Tokgöz-Yılmaz, Burcu Öztürk Hişmi, Hi̇lal Özdağ,

The American Journal of Human Genetics

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiologyMolecular GeneticsTruncating MutationDisease Gene IdentificationCochlear DevelopmentSerpinb6 IsMedical GeneticsArtsMedicineHearing Loss

References

	Year	Citations

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