Related content

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation

By Doss Sarah   Lohmann Katja   Seibler Philip   Arns Björn   Klopstock Thomas   Zühlke Christine   Freimann Karen   Winkler Susen   Lohnau Thora   Drungowski Mario   Nürnberg Peter   Wiegers Karin   Lohmann Ebba   Naz Sadaf   Kasten Meike   Bohner Georg   Ramirez Alfredo   Endres Matthias   Klein Christine  

Journal of Neurology, Vol. 261, Iss. 1, 2014-01 ,pp. : 207-212

Springer Publishing Company

Access to resources Recommend Favorite

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome

By Bassuk A.   Chen Y.   Batish S.   Nagan N.   Opal P.   Chance P.   Bennett C.  

Neurogenetics, Vol. 8, Iss. 1, 2007-01 ,pp. : 45-49

Springer Publishing Company

Access to resources Recommend Favorite

A truncating mutation in B3GNT1 causes severe Walker–Warburg syndrome

By Shaheen Ranad   Faqeih Eissa   Ansari Shinu   Alkuraya Fowzan  

Neurogenetics, Vol. 14, Iss. 3-4, 2013-11 ,pp. : 243-245

Springer Publishing Company

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease)

By Rub U.   Brunt E.R.   Gierga K.   Schultz C.   Paulson H.   de Vos R.A.I.   Braak H.  

Journal of Chemical Neuroanatomy, Vol. 25, Iss. 2, 2003-02 ,pp. : 115-127

Elsevier

Access to resources Recommend Favorite