A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.
- DOI
- 10.1016/j.jns.2014.10.018
- Published
- 2014 Dec 15
- Container
- Journal of the neurological sciences
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.jns.2014.10.018,
title = {A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.},
author = {Jahic A and Kreuz F and Zacher P and Fiedler J and Bier A and Reif S and Rieger M and Krüger S and Beetz C and Plaschke J},
year = {2014},
journal = {Journal of the neurological sciences},
doi = {10.1016/j.jns.2014.10.018},
url = {https://doi.org/10.1016/j.jns.2014.10.018}
}RIS
TY - JOUR TI - A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8. AU - Jahic A AU - Kreuz F AU - Zacher P AU - Fiedler J AU - Bier A AU - Reif S AU - Rieger M AU - Krüger S AU - Beetz C AU - Plaschke J PY - 2014 JO - Journal of the neurological sciences DO - 10.1016/j.jns.2014.10.018 UR - https://doi.org/10.1016/j.jns.2014.10.018 ER -
APA
A, J., F, K., P, Z., J, F., A, B., S, R., M, R., S, K., C, B., & J, P. (2014). A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.. Journal of the neurological sciences. https://doi.org/10.1016/j.jns.2014.10.018
Source records
- pubmed · retrieved 2026-09-25T18:09:16.724Z