M. Ichiba

A gene‐targeted mouse model for chorea‐acanthocytosis

Daisuke Sato, Kenji Nakamura, M. Katsuki, 2005, Journal of neurochemistry.

Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms

A. Sano, S. Ueno, I. Higuchi, 2011, Neuroscience Research.

Different Clinical Phenotypes in Siblings with a Presenilin-1 P264L Mutation

S. Fujita, K. Takeuchi, A. Sano, 2012, Dementia and Geriatric Cognitive Disorders.

Chorea-acanthocytosis with upper motor neuron degeneration and 3419_3420 delCA and 3970_3973 delAGTC VPS13A mutations

K. Wakabayashi, F. Mori, A. Sano, 2010, Acta Neuropathologica.

Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea‐acanthocytosis

K. Kotschet, D. Babovic‐Vuksanovic, K. Wakabayashi, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

In vivo distribution and localization of chorein.

S. Izumo, A. Sano, Masayuki Nakamura, 2007, Biochemical and biophysical research communications.

Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree

A. Sano, Masayuki Nakamura, Y. Tomemori, 2007, Journal of the Neurological Sciences.

A new phenotype of chorea‐acanthocytosis with dilated cardiomyopathy and myopathy

Keiji Matsumoto, A. Sano, S. Ueno, 2007, Movement disorders : official journal of the Movement Disorder Society.

Familial Semantic Dementia with P301L Mutation in the Tau Gene

A. Sano, Masayuki Nakamura, M. Ichiba, 2011, Dementia and Geriatric Cognitive Disorders.

Adult‐type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case

K. Arimura, A. Sano, Y. Okamoto, 2011, Psychiatry and clinical neurosciences.

Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia

A. Sano, S. Ueno, Masayuki Nakamura, 2011, Neuroscience Research.

Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C.

A. Sano, Masayuki Nakamura, M. Ichiba, 2007, Biochemical and biophysical research communications.

Chorein deficiency leads to upregulation of gephyrin and GABA(A) receptor.

S. Izumo, A. Sano, Masayuki Nakamura, 2006, Biochemical and biophysical research communications.

A Mouse Model of Chorea-Acanthocytosis

Y. Katoh, A. Sano, S. Ueno, 2008 .

Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea‐acanthocytosis

K. Kotschet, D. Babovic‐Vuksanovic, K. Wakabayashi, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.