Publication | Closed Access
Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients
45
Citations
34
References
2005
Year
Mendelian DisorderGenetic DisorderGeneticsAudiologyGjb2 MutationsPathologyDisease Gene IdentificationCochlear DevelopmentArtsMedicineVariant InterpretationHearing Loss
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