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35delg mutation
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EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
2013 |
Second Faculty of Medicine
publication
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness
2004 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport