The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.


OLGIATI S., DOĞU O., TUFEKCIOGLU Z., DILER Y., SAKA E., GULTEKIN M. H., ...Daha Fazla

Parkinsonism & related disorders, cilt.39, ss.64-70, 2017 (SCI-Expanded) identifier identifier identifier