Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up.

Durmus H., Shen X., Serdaroglu-Oflazer P., Kara B., Parman-Gulsen Y., Ozdemir C., ...Daha Fazla

Neuromuscular disorders : NMD, cilt.28, ss.315-322, 2018 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 28
  • Basım Tarihi: 2018
  • Doi Numarası: 10.1016/j.nmd.2017.11.013
  • Dergi Adı: Neuromuscular disorders : NMD
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.315-322
  • Anahtar Kelimeler: Congenital myasthenic syndromes, Turkey, Genetic, Myasthenia, PLATE ACETYLCHOLINESTERASE DEFICIENCY, NEUROMUSCULAR-JUNCTION SYNAPTOPATHY, COLQ MUTATION, RECEPTOR, CHANNEL, HETEROGENEITY, GENE, TRANSMISSION, DEFECTS
  • Kocaeli Üniversitesi Adresli: Evet