Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis.
AUTHORS
Erlich
YYaniv ,
Edvardson
S Simon ,
Hodges
E Emily ,
Zenvirt
S Shamir ,
Thekkat
P Pramod ,
Shaag
A Avraham ,
Dor
T Talya ,
Hannon
GJ Gregory J ,
Elpeleg
O Orly .
Genome research. 2011 5 ; 21(5).
658-64
- PMID: 21487076[PubMed].
- PMCID: PMC3083082.