(Q28286077)

A Sousa

8

0 references

Cristina Santos

C Santos

5

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Rafael Montiel

R Montiel

3

0 references

Paula Coutinho

P Coutinho

10

0 references

Conceicao Bettencourt

C Bettencourt

7

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Manuela Lima

M Lima

1

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Patricia Maciel

P Maciel

11

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author name string

M C Costa

2

0 references

C Silva

6

0 references

J Sequeiros

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

9

0 references

language of work or name

English

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publication date

2005

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published in

Human Heredity

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volume

60

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issue

3

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page(s)

156-63

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cites work

1 reference

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

21 January 2018

1 reference

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

21 January 2018

1 reference

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

21 January 2018

1 reference

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

21 January 2018

1 reference

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

21 January 2018

1 reference

The gene for Machado-Joseph disease maps to human chromosome 14q

21 January 2018

1 reference

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

21 January 2018

1 reference

Disease knowledge and attitudes toward predictive testing and prenatal diagnosis in families with Machado-Joseph disease from the Azores Islands (Portugal).

21 January 2018

1 reference

Improvement in the molecular diagnosis of Machado-Joseph disease

21 January 2018

1 reference