Search Results - AlAsmari, Ali
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A reverse genetics and genomics approach to gene paralog function and disease: myokymia and the juxtaparanode by Marafi, Dana (Author) , Kozar, Nina (Author) , Duan, Ruizhi (Author) , Bradley, Stephen (Author) , Yokochi, Kenji (Author) , Al Mutairi, Fuad (Author) , Saadi, Nebal Waill (Author) , Whalen, Sandra (Author) , Brunet, Theresa (Author) , Kotzaeridou, Urania (Author) , Choukair, Daniela (Author) , Keren, Boris (Author) , Nava, Caroline (Author) , Kato, Mitsuhiro (Author) , Arai, Hiroshi (Author) , Froukh, Tawfiq (Author) , Faqeih, Eissa Ali (Author) , AlAsmari, Ali M. (Author) , Saleh, Mohammed M. (Author) , Pinto e Vairo, Filippo (Author) , Pichurin, Pavel N. (Author) , Klee, Eric W. (Author) , Schmitz, Christopher T. (Author) , Grochowski, Christopher M. (Author) , Mitani, Tadahiro (Author) , Herman, Isabella (Author) , Calame, Daniel G. (Author) , Fatih, Jawid M. (Author) , Du, Haowei (Author) , Coban-Akdemir, Zeynep (Author) , Pehlivan, Davut (Author) , Jhangiani, Shalini N. (Author) , Gibbs, Richard A. (Author) , Miyatake, Satoko (Author) , Matsumoto, Naomichi (Author) , Wagstaff, Laura J. (Author) , Posey, Jennifer E. (Author) , Lupski, James R. (Author) , Meijer, Dies (Author) , Wagner, Matias (Author) ,
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Succinyl-CoA:3-oxoacid coenzyme a transferase (SCOT) deficiency: a rare and potentially fatal metabolic disease by Grünert, Sarah (Author) , Foster, William (Author) , Schumann, Anke (Author) , Lund, Allan (Author) , Pontes, Christina (Author) , Roloff, Sylvia (Author) , Weinhold, Natalie (Author) , Yue, Wyatt W. (Author) , AlAsmari, Ali (Author) , Obaid, Osama A. (Author) , Faqeih, Eissa Ali (Author) , Stübbe, Lisa (Author) , Yamamoto, Raina (Author) , Gemperle-Britschgi, Corinne (Author) , Walter, Melanie (Author) , Spiekerkoetter, Ute (Author) , Mackinnon, Sabrina (Author) , Sass, Jörn Oliver (Author) ,
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Related Subjects
Inborn error of metabolism
KCNA
Ketoacidosis
Ketolysis
Ketone body utilization
LGI3
Metabolic acidosis
bi-allelic variation
facial myokymia
gene and genome instability
genomic rearrangement
multi-exonic CNV
neurobiology of disease
peripheral nerve hyperexcitability syndromes
potassium channel complexes