Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1- mutation due to uniparental disomy
Kurth, Ingo, Baumgartner, Manuela, Schabhüttl, Maria, Tomni, Cecilia, Windhager, Reinhard, Strom, Tim M., Wieland, Thomas, Gremel, Kurt, Auer-Grumbach, MichaelaLanguage:
english
Journal:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
DOI:
10.1002/ajmg.b.32458
Date:
May, 2016
File:
PDF, 589 KB
english, 2016