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机译:
Department of Clinical Biochemistry, Faculty of Medicine, King Abdulaziz University;
b Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University;
Deptartment of Genetics, Bhagwan Mahavir Medical Research CentreDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud UniversityDepartment of PharmacologyandToxicology, Faculty of Pharmacy, King Abdulaziz UniversityDepartment of Entomology, Rutgers Universityg Deanship of Scientific Research, King Abdulaziz UniversityPrincess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz Universityh Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University;
KCNH2 gene; missense mutations; deleteriousness; 3D modeling; stability;
机译:Genetic interaction analysis of point mutations enables interrogation of gene function at a residue-level resolution Exploring the applications of high-resolution genetic interaction mapping of point mutations
机译:Improved single-step enrichment methods of cross-linked products for protein structure analysis and protein interaction mapping
机译:Genetic homogeneity, high-resolution mapping, and mutation analysis of the urofacial (Ochoa) syndrome and exclusion of the glutamate oxaloacetate transaminase gene (GOT1) in the critical region as the disease gene