(Q86123986)
Statements
A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8 (English)
Amir Jahic
Friedmar Kreuz
Pia Zacher
Jana Fiedler
Andrea Bier
Silke Reif
Manuela Rieger
Stefan Krüger
16 October 2014