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M Spadaro

Showing results (61-70 of 65) with videos related to

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American Journal of Human Genetics|July 1, 1991
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindredsH Y Zoghbi, C Jodice, L A Sandkuijl, et al.
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.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
American Journal of Human Genetics|July 1, 1991
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindredsH Y Zoghbi, C Jodice, L A Sandkuijl, et al.
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.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Pageof 7