Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum

J Neurol. 2016 Oct;263(10):2130-2. doi: 10.1007/s00415-016-8258-1. Epub 2016 Aug 20.

Authors

Sanjiban Chakrabarty¹, Nimish Vijayakumar², Kurupath Radhakrishnan², Kapaettu Satyamoorthy³

Affiliations

¹ Department of Cell and Molecular Biology, School of Life Sciences, Manipal University, Manipal, Karnataka, 576104, India.
² Department of Neurology, Kasturba Medical College, Manipal University, Manipal, Karnataka, 576104, India.
³ Department of Cell and Molecular Biology, School of Life Sciences, Manipal University, Manipal, Karnataka, 576104, India. ksatyamoorthy@manipal.edu.

PMID: 27544497
DOI: 10.1007/s00415-016-8258-1

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Agenesis of Corpus Callosum / complications*
Agenesis of Corpus Callosum / diagnostic imaging
Carrier Proteins / genetics*
Consanguinity
Corpus Callosum / diagnostic imaging
DNA Mutational Analysis
Female
Humans
Magnetic Resonance Imaging
Mutation / genetics*
Spastic Paraplegia, Hereditary / complications*
Spastic Paraplegia, Hereditary / diagnostic imaging
Spastic Paraplegia, Hereditary / genetics*
Young Adult

Substances

Carrier Proteins
ZFYVE26 protein, human

Supplementary concepts

Partial agenesis of corpus callosum