RGD Reference Report - Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10. - Rat Genome Database
Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10.

Authors: Carosi, Laura  Lo Giudice, Temistocle  Di Lullo, Martina  Lombardi, Federica  Babalini, Carla  Gaudiello, Fabrizio  Marfia, Girolama Alessandra  Massa, Roberto  Kawarai, Toshitaka  Orlacchio, Antonio 
Citation: Carosi L, etal., J Neurol Neurosurg Psychiatry. 2015 Jun;86(6):702-4. doi: 10.1136/jnnp-2014-308625. Epub 2014 Oct 28.
RGD ID: 12793068
Pubmed: (View Article at PubMed) PMID:25352184
DOI: Full-text: DOI:10.1136/jnnp-2014-308625

Abstract for this paper unavailable

Annotation

Disease Annotations    

Objects Annotated

Genes (Rattus norvegicus)
Kif5a  (kinesin family member 5A)

Genes (Mus musculus)
Kif5a  (kinesin family member 5A)

Genes (Homo sapiens)
KIF5A  (kinesin family member 5A)


Additional Information