C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment

BACKGROUND: C.35delG/GJB2 mutation is the most frequent genetic cause of deafness in Caucasians. Another frequent mutation in some Caucasian populations is del(GJB6-D13S1830). Both GJB2 and GJB6 genes belong to the same DFNB1 locus and when the two mutations are found in combination in a hearing-imp...

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Detalles Bibliográficos
Autores principales: Medica, Igor, Rudolf, Gorazd, Balaban, Manuela, Peterlin, Borut
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325043/
https://www.ncbi.nlm.nih.gov/pubmed/16336662
http://dx.doi.org/10.1186/1472-6815-5-11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325043/
https://www.ncbi.nlm.nih.gov/pubmed/16336662
http://dx.doi.org/10.1186/1472-6815-5-11

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