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Epilepsy Research
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January 25, 2015
Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras
Emanuela Dazzo, Lia Santulli, Annio Posar, et al.
Frontiers in Genetics
|
November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder
Leonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Epilepsy Research
|
February 22, 2011
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
Giorgia Busolin, Sandro Malacrida, Francesca Bisulli, et al.
American Journal of Human Genetics
|
July 16, 2024
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes
Dmitrijs Rots, Sanaa Choufani, Victor Faundes, et al.
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Search research articles
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Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
Epilepsy Research
|
January 25, 2015
Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras
Emanuela Dazzo, Lia Santulli, Annio Posar, et al.
Frontiers in Genetics
|
November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder
Leonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Epilepsy Research
|
February 22, 2011
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
Giorgia Busolin, Sandro Malacrida, Francesca Bisulli, et al.
American Journal of Human Genetics
|
July 16, 2024
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes
Dmitrijs Rots, Sanaa Choufani, Victor Faundes, et al.
Page
of 6