Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

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Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

@yue

2012年論文

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2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

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2012年论文

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2012年论文

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Analysis of autosomal dominant ...... tended family of central India

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type

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Analysis of autosomal dominant ...... tended family of central India

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Analysis of autosomal dominant ...... tended family of central India

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P1476

Analysis of autosomal dominant ...... tended family of central India

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P2093

Ajaypal Singh

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Kishore B Lowalekar

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Manoj Singh Rohilla

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Pramod Kumar Tiwari

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Satish S Poojary

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Shashikant Sharma

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Tekcham Dinesh Singh

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P2860

Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1

Trinucleotide Repeat Disorders

A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis.

Glutamine repeats and neurodegeneration.

The ins and outs of a polyglutamine neurodegenerative disease: spinocerebellar ataxia type 1 (SCA1).

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

SCA1 molecular genetics: a history of a 13 year collaboration against glutamines.

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Pathogenesis of polyglutamine disorders: aggregation revisited.

P304

299-304

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P31

scholarly article

P356

10.4103/0971-6866.107981

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P433

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P478

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P577

2012-09-01T00:00:00Z

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P5875

236959029

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P698

23716937

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P932

3656518

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