Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients - Concepedia

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Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients

78

Citations

21

References

2002

Year

Marie Wattenhofer‐Donzé, Mario Iorio, Raquel Rabionet, Loretta Dougherty, Torsten Schwede, Bàrbara Montserrat-Sentís, María L. Arbonés, Theofilos Iliades, Annamaria Pasquadibisceglie, Marcello D’Amelio,

Journal of Molecular Medicine

Tmprss3 GeneChildhood Nonsyndromic DeafnessPediatric OtolaryngologyGenetic DisorderGeneticsGenetic EpidemiologyPediatricsAudiologyCaucasian PatientsCochlear DevelopmentArtsMedicineHearing Loss

References

	Year	Citations

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