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Neurology
|
May 11, 2016
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
Johannes R Lemke, Kirsten Geider, Katherine L Helbig, et al.
Genome Medicine
|
June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome
Margot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
Brain : a Journal of Neurology
|
February 9, 2023
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
Afshin Saffari, Tracy Lau, Homa Tajsharghi, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 23) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 23 results.
Neurology
|
May 11, 2016
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
Johannes R Lemke, Kirsten Geider, Katherine L Helbig, et al.
Genome Medicine
|
June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome
Margot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
Brain : a Journal of Neurology
|
February 9, 2023
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
Afshin Saffari, Tracy Lau, Homa Tajsharghi, et al.
Page
of 3