Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.

Vanmolkot K., Kors E., Turk U., Turkdogan D., Keyser A., Broos L., ...Daha Fazla

European journal of human genetics : EJHG, cilt.14, ss.555-60, 2006 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 14
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1038/sj.ejhg.5201607
  • Dergi Adı: European journal of human genetics : EJHG
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.555-60
  • Anahtar Kelimeler: familial hemiplegic migraine (FHM), ATP1A2, Na, K-ATPase, CALCIUM-CHANNEL, ALTERNATING HEMIPLEGIA, SARCOPLASMIC-RETICULUM, ALPHA-SUBUNIT, TYPE-2, NA,K-ATPASE, PUMP, CHILDHOOD, ISOFORM, DOMAIN
  • Marmara Üniversitesi Adresli: Evet