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Mutation in gap and tight junctions in patients with non-syndromic hearing loss
Biochemical and Biophysical Research Communications, 06/05/09
Belguith H et al. - The study confirms the importance of GJB2 screening in ARNSHI and suggests that in consanguineous populations, a single DFNB1 mutant allele in individuals with HI is likely due to a coincidental carrier state.
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Today in Basic Science/Genetics...keeping you current
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Today in Otology/Neurotology...keeping you current
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New Patterns in the Otopathogens Causing Acute Otitis Media Six to Eight Years After Introduction of Pneumococcal Conjugate Vaccine
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