Funder
Manchester Biomedical Research Centre
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Otorhinolaryngology,Pathology and Forensic Medicine
Reference22 articles.
1. Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, et al. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction. Hum Mol Genet. 2006;15(7):1071–85.
https://doi.org/10.1093/hmg/ddl022
.
2. Ikezono T, Omori A, Ichinose S, Pawankar R, Watanabe A, Yagi T. Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein. Biochem Biophys Acta. 2001;1535(3):258–65.
3. Robertson NG, O’Malley JT, Ong CA, Giersch AB, Shen J, Stankovic KM, et al. Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice. J Assoc Res Otolaryngol. 2014;15(6):961–74.
https://doi.org/10.1007/s10162-014-0481-9
.
4. Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, et al. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. Nat Genet. 1998;20(3):299–303.
https://doi.org/10.1038/3118
.
5. Khetarpal U, Schuknecht HF, Gacek RR, Holmes LB. Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds. Arch Otolaryngol-Head Neck Surg. 1991;117(9):1032–42.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献