A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment - Concepedia

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Publication | Open Access

A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

DOI Full Paper Access

134

Citations

27

References

2012

Year

Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar, Maria Magdalena Picher, Manou Sommen, Celia Zazo Seco, Jaap Oostrik, Hannie Kremer,

The American Journal of Human Genetics

Autosomal-recessive Hearing ImpairmentDevelopmental BiologyHealth SciencesGenetic DisorderGeneticsAuditory PhysiologyCochlear PhysiologyMolecular GeneticsCochlear DevelopmentAuditory ResearchAuditory ScienceHuman HearingMedicineAuditory SystemCochlear Hair CellsAuditory Hair CellsHearing Loss

References

	Year	Citations

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