Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: - exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant

By Knight M.A.   Kennerson M.L.   Anney R.J.   Matsuura T.   Nicholson G.A.   Salimi-Tari P.   Gardner R.J.M.   Storey E.   Forrest S.M.  

Neurobiology of Disease, Vol. 13, Iss. 2, 2003-07 ,pp. : 147-157

Elsevier

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A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23

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Brain, Vol. 126, Iss. 6, 2003-06 ,pp. : 1293-1299

Oxford University Press

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Visual loss as the presenting sign in spinocerebellar ataxia type 7 (SCA 7 )

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Neuro-Ophthalmology, Vol. 28, Iss. 5-6, 2004-11 ,pp. : 265-271

Informa Healthcare

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Episodic see-saw nystagmus in spinocerebellar ataxia type 2 (SCA-2)

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The Cerebellum, Vol. 1, Iss. 1, 2002-01 ,pp. : 91-92

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Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance

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Brain, Vol. 126, Iss. 10, 2003-10 ,pp. : 2257-2272

Oxford University Press

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