A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8 (Q86123986)
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scientific article published on 16 October 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8 |
scientific article published on 16 October 2014 |
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