Literature DB >> 17987652

Association of spinocerebellar ataxia type 3 and spinocerebellar ataxia type 8 microsatellite expansions: genetic counseling implications.

Sabrina Paganoni, Christina A Seelaus, Kelly E Ormond, Puneet Opal.   

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Year:  2008        PMID： 17987652     DOI： 10.1002/mds.21797

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  4 in total

1.  Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias.

Authors:  Jorge Sequeiros; Sara Seneca; Joanne Martindale
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

2.  Spinocerebellar Ataxia 2 and 12 Mutations in an Indian Family with Cerebellar Ataxia and Slow Saccades.

Authors:  Mohammed Faruq; Sunil Shakya; Ajay Garg; Achal Kumar Srivastava
Journal:  Mov Disord Clin Pract       Date:  2014-07-31

3.  Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.

Authors:  J F Baizabal-Carvallo; G Xia; P Botros; J Laguna; T Ashizawa; J Jankovic
Journal:  Acta Neurol Scand       Date:  2015-01-28       Impact factor: 3.209

4.  A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.

Authors:  Pooja Sharma; Akhilesh K Sonakar; Vinay Goel; Ajay Garg; Achal K Srivastava; Mohammed Faruq
Journal:  Mov Disord Clin Pract       Date:  2022-05-10
  4 in total

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