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Barry Chioza

Showing results (11-20 of 15) with videos related to

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Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
The EMBO Journal|March 14, 2013
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative diseaseReza Sharifi, Rosa Morra, C Denise Appel, et al.
Brain : a Journal of Neurology|October 10, 2013
Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesisGaurav V Harlalka, Anna Lehman, Barry Chioza, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
The EMBO Journal|March 14, 2013
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative diseaseReza Sharifi, Rosa Morra, C Denise Appel, et al.
Brain : a Journal of Neurology|October 10, 2013
Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesisGaurav V Harlalka, Anna Lehman, Barry Chioza, et al.
Pageof 2