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High prevalence of the IVS 1 + 1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2
P Seeman, I SakmaryováVolume:
69
Year:
2006
Language:
english
Pages:
4
DOI:
10.1111/j.1399-0004.2006.00602.x
File:
PDF, 84 KB
english, 2006