The c.IVS1+1G > A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

Sirmaci A., Akcayoz-Duman D., Tekin M.

JOURNAL OF GENETICS, cilt.85, sa.3, ss.213-216, 2006 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 85 Sayı: 3
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1007/bf02935334
  • Dergi Adı: JOURNAL OF GENETICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.213-216
  • Anahtar Kelimeler: connexin26, connexin30, deafness, gap junctions, GJB2, GJB6, hearing impairment, SYNDROMIC HEARING-LOSS, CONNEXIN-26 35DELG, IMPAIRMENT, DEAFNESS, FREQUENCY, ORIGINS
  • Ankara Üniversitesi Adresli: Hayır