Linkage analysis of hearing impairment in families of Bannu Distric

Farmanullah F., Khan J., Ismail M., Rafi M., Ehsanullah E., Jalal A.

JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, cilt.69, sa.11, ss.1632-1636, 2019 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 69 Sayı: 11
  • Basım Tarihi: 2019
  • Doi Numarası: 10.5455/jpma.300796
  • Dergi Adı: JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1632-1636
  • Anahtar Kelimeler: Congenital deafness, Linkage, Touch-down PCR, Haplogroup, USHER-SYNDROME, MOUSE MODEL, MUTATIONS, DEAFNESS, MYO15A, GENETICS, CDH23
  • İstanbul Üniversitesi Adresli: Hayır

Özet

Objective: To link congenital hearing loss with known loci to establish a platform for future research.