A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport.

Wang L, Brown A

DOI: 10.1186/1750-1326-5-52
Published: 2010 Nov 18
Container: Molecular neurodegeneration
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/1750-1326-5-52,
  title = {A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport.},
  author = {Wang L and Brown A},
  year = {2010},
  journal = {Molecular neurodegeneration},
  doi = {10.1186/1750-1326-5-52},
  url = {https://doi.org/10.1186/1750-1326-5-52}
}

RIS

TY  - JOUR
TI  - A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport.
AU  - Wang L
AU  - Brown A
PY  - 2010
JO  - Molecular neurodegeneration
DO  - 10.1186/1750-1326-5-52
UR  - https://doi.org/10.1186/1750-1326-5-52
ER  -

APA

L, W., & A, B. (2010). A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport.. Molecular neurodegeneration. https://doi.org/10.1186/1750-1326-5-52

Source records

pubmed · retrieved 2026-09-25T23:47:55.134Z