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R Stucka

Showing results (31-40 of 37) with videos related to

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Journal of Medical Genetics|August 3, 2004
The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founderJ S Müller, A Abicht, G Burke, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Human Molecular Genetics|December 26, 2001
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblastsM Jaksch, C Paret, R Stucka, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Molecular characterisation of congenital myasthenic syndromes in Southern BrazilV Mihaylova, R H Scola, B Gervini, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
Journal of Medical Genetics|April 3, 2004
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patientsM C Walter, J A Petersen, R Stucka, et al.
The EMBO Journal|December 15, 1994
Complete DNA sequence of yeast chromosome IIH Feldmann, M Aigle, G Aljinovic, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Journal of Medical Genetics|August 3, 2004
The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founderJ S Müller, A Abicht, G Burke, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Human Molecular Genetics|December 26, 2001
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblastsM Jaksch, C Paret, R Stucka, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Molecular characterisation of congenital myasthenic syndromes in Southern BrazilV Mihaylova, R H Scola, B Gervini, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
Journal of Medical Genetics|April 3, 2004
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patientsM C Walter, J A Petersen, R Stucka, et al.
The EMBO Journal|December 15, 1994
Complete DNA sequence of yeast chromosome IIH Feldmann, M Aigle, G Aljinovic, et al.
Pageof 4