Skip to Main Content

Paper Details

BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood.
Am J Med Genet A
24
2016
Author NameAffiliation
Denise HornInstitut fur Medizinische Genetik und Humangenetik, Charite-Universitatsmedizin Berlin
Bj??rn Fischer-ZirnsakInstitut fur Medizinische Genetik und Humangenetik, Charite-Universitatsmedizin Berlin
Bj??rn Fischer-ZirnsakMax-Planck-Institut fur Molekulare Genetik
Tomasz ZemojtelInstitute of Bioorganic Chemistry, Polish Academy of Sciences
Tomasz Zemojtel
  • 1 - 5

Datasets

Release 1.2