P. Seeman
Department of Child Neurology
DNA Laboratory
Charles University Prague
2nd School of Medicine
Czech Republic
Name/email consistency: high
- 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. Seeman, P., Sakmaryová, I. Clin. Genet. (2006)