Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2

The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2K

(2010) C. Crimella et al.   JOURNAL OF MEDICAL GENETICS

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

(2010) Lina Wang et al.   Molecular Neurodegeneration

Kinesin superfamily motor proteins and intracellular transport

(2009) Nobutaka Hirokawa et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity

(2008) Bettina Ebbing et al.   HUMAN MOLECULAR GENETICS

Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10

(2008) Cyril Goizet et al.   HUMAN MUTATION

A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy

(2008) A. Tessa et al.   JOURNAL OF NEUROLOGY

SPG10 is a rare cause of spastic paraplegia in European families

(2008) R Schule et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The role of microtubules in processive kinesin movement

(2008) Masahide Kikkawa   TRENDS IN CELL BIOLOGY