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Year | Number of Results |
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2005 | 1 |
2013 | 1 |
2014 | 1 |
2025 | 0 |
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SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.
J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208.
J Med Genet. 2005.
PMID: 15689455
Free PMC article.
No abstract available.
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.
Chattaraj P, Reimold FR, Muskett JA, Shmukler BE, Chien WW, Madeo AC, Pryor SP, Zalewski CK, Butman JA, Brewer CC, Kenna MA, Alper SL, Griffith AJ.
Chattaraj P, et al.
JAMA Otolaryngol Head Neck Surg. 2013 Sep;139(9):907-13. doi: 10.1001/jamaoto.2013.4185.
JAMA Otolaryngol Head Neck Surg. 2013.
PMID: 24051746
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Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type C.
King KA, Gordon-Salant S, Pawlowski KS, Taylor AM, Griffith AJ, Houser A, Kurima K, Wassif CA, Wright CG, Porter FD, Repa JJ, Brewer CC.
King KA, et al.
J Assoc Res Otolaryngol. 2014 Aug;15(4):529-41. doi: 10.1007/s10162-014-0459-7. Epub 2014 May 17.
J Assoc Res Otolaryngol. 2014.
PMID: 24839095
Free PMC article.
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