A Phenotype Resembling the Clouston Syndrome with Deafness Is Associated with a Novel Missense GJB2 Mutation - Concepedia

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A Phenotype Resembling the Clouston Syndrome with Deafness Is Associated with a Novel Missense GJB2 Mutation

DOI Full Paper Access

48

Citations

7

References

2004

Year

Maurice A. M. Van Steensel, Peter M. Steijlen, Reno S. Bladergroen, Elisabeth H. Hoefsloot, Connie M. van Ravenswaaij-Arts, Michel van Geel

Journal of Investigative Dermatology

Deafness Is AssociatedGenetic DisorderGeneticsPathogenesisClouston SyndromePathologyMolecular GeneticsDisease Gene IdentificationCochlear DevelopmentMedicine

References

	Year	Citations

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