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المؤلفون: Peter Nürnberg, Tobias Eisenberger, Dirk Mürbe, Christian Decker, Nataliya Di Donato, Mohammad R. Toliat, Andrea Delle Vedove, Christine Neuhaus, Gudrun Nürnberg, Hanno J. Bolz
المصدر: Genetics in Medicine
مصطلحات موضوعية: Male, 0301 basic medicine, deafness, DFNB84A, Genetic Linkage, Nonsense mutation, nonsense mutation, Genome-wide association study, Deafness, autosomal-dominant hearing loss, Biology, medicine.disease_cause, 03 medical and health sciences, Exon, symbols.namesake, Genetic linkage, Exome Sequencing, medicine, Humans, Exome, Family, Amino Acid Sequence, Original Research Article, Allele, Hearing Loss, PTPRQ, Genetics (clinical), Exome sequencing, Genetics, Sanger sequencing, Mutation, Receptor-Like Protein Tyrosine Phosphatases, Class 3, Exons, Pedigree, 030104 developmental biology, Codon, Nonsense, symbols, Female, Genome-Wide Association Study
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2دورية أكاديمية
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