Genomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease

ENDER K., PEHLİVAN D., TA H., SM W., HM S., GAMBIN T., ...Daha Fazla

american society of human genetics, 18 - 22 Ekim 2014

  • Yayın Türü: Bildiri
  • İstanbul Üniversitesi Adresli: Hayır