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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

✍ Scribed by P Seeman; I Sakmaryová

Book ID: 110888185
Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 84 KB
Volume: 69
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2006.00602.x

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