High prevalence of IVS1+1 to G>A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2

• SEEMAN P.

収録刊行物

• Clin. Genet.

  Clin. Genet. 69 410-413, 2006

詳細情報

• CRID: 1570291225840842752
• NII論文ID: 10030660775
• データソース種別:
  • CiNii Articles