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Journal Article|Research Support, Non-U.S. Gov't |
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873 |
| issn |
0165-5876 |
| issueIdentifier |
6 |
| pageRange |
869-873 |
| publicationName |
International Journal of Pediatric Otorhinolaryngology |
| startingPage |
869 |
| bibliographicCitation |
Esmaeili M, Bonyadi M, Nejadkazem M. Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness. International Journal of Pediatric Otorhinolaryngology. 2007 Jun;71(6):869–73. doi: 10.1016/j.ijporl.2007.02.007. |
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| date |
200706 |
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https://pubmed.ncbi.nlm.nih.gov/17368814
https://doi.org/10.1016/j.ijporl.2007.02.007 |
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https://portal.issn.org/resource/ISSN/0165-5876 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness |
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