检索结果 - Alexandra Lissouba
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia 由 Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B. Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B. Laurent, Daniel Rochefort, Dan Spiegelman, Alexandre Dionne‐Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed Yahyaoui, Réda Ouazzani, Grace Yoon, Nicolas Dupré, Oksana Suchowersky, François V. Bolduc, J. Alex Parker, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau, Bouchra Ouled Amar Bencheikh
出版 2016Artigo
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Biology
Gene
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Amyotrophic lateral sclerosis
CRISPR
Computational biology
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Hereditary spastic paraplegia
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Pathology
Cas9
DNA microarray
DNA repair
Danio
Disease gene identification
Embryo
Exome sequencing
Frameshift mutation
Gene expression
Gene knockdown
Genome
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High Resolution Melt
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Homology (biology)