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- Minoshima, S
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- Foster, N L
Producer: 20041026
In:
Neurology vol. 62
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KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction. [electronic resource] by
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- Durr, Alexandra
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- Benomar, Ali
- Stevanin, Giovanni
- Schuelke, Markus
- Edvardson, Simon
Producer: 20140908
In:
Journal of medical genetics vol. 51
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A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation. [electronic resource] by
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- Kugimoto, Chiharu
- Ueda, Naohisa
- Hirata, Junichi
- Tomita-Katsumoto, Atsuko
- Kashikura-Kojima, Mari
- Kubota, Shun
- Taniguchi, Midori
- Murayama, Kei
- Nakashima, Mitsuko
- Tsurusaki, Yoshinori
- Miyake, Noriko
- Saitsu, Hirotomo
- Matsumoto, Naomichi
- Tanaka, Fumiaki
Producer: 20151009
In:
Journal of human genetics vol. 60
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400.
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