Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.

Tunca C., Şeker T., Akçimen F., Coşkun C., Bayraktar E., Palvadeau R., ...Daha Fazla

Human mutation, cilt.41, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 41
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1002/humu.24055
  • Dergi Adı: Human mutation
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, EMBASE, MEDLINE
  • Anahtar Kelimeler: ALS, ALS variant database, genetics, clinical exome sequencing, coexpression network analysis, genetics, genome-wide association study, motor neuron disease, next generation sequencing, Turkish peninsula, AMYOTROPHIC-LATERAL-SCLEROSIS, MOTOR-NEURON DISEASE, SPINAL MUSCULAR-ATROPHY, CELL-CYCLE REGULATORS, COEXPRESSION NETWORK, SEQUENCE VARIATION, ANALYSES IDENTIFY, GENE-MUTATIONS, RISK, FORM
  • Çukurova Üniversitesi Adresli: Evet