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M Frontali

Showing results (41-50 of 47) with videos related to

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Human Molecular Genetics|September 25, 1997
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19pC Jodice, E Mantuano, L Veneziano, et al.
Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.
American Journal of Human Genetics|February 17, 2001
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2S Guida, F Trettel, S Pagnutti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.
Neurology|February 11, 2012
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionJ-M Lee, E M Ramos, J-H Lee, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Human Molecular Genetics|September 25, 1997
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19pC Jodice, E Mantuano, L Veneziano, et al.
Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.
American Journal of Human Genetics|February 17, 2001
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2S Guida, F Trettel, S Pagnutti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.
Neurology|February 11, 2012
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionJ-M Lee, E M Ramos, J-H Lee, et al.
Pageof 5