المؤلفون: M-J Clermont, Seza Ozen, G Li Volti, Cynthia C. Morton, Sally A. Hulton, H Kroes, E. Al-Sabban, Aysin Bakkaloglu, E H Stover, Sami A. Sanjad, Sevgi Mir, N Eady, C Bavalia, Ipek Akil, Anne Giersch, D M Fritz, Velibor Tasic, David M. Baguley, Zelal Bircan, H Mocan, Ahmet Nayir, A Guala, D Chauveau, Charlotte M. Taylor, Annabel N. Smith, Fiona E. Karet, P R Axon, J Rodriguez Soriano, Nanyawan Rungroj, Sebastiano Bianca, Rezan Topaloglu, Katherine J. Borthwick

المساهمون: Çocuk Sağlığı ve Hastalıkları, Ege Üniversitesi

المصدر: JOURNAL OF MEDICAL GENETICS, 39(11), 796-803. BMJ PUBLISHING GROUP

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Genotype, Genetic Linkage, Hearing loss, Hearing Loss, Sensorineural, DNA Mutational Analysis, Genes, Recessive, Single-nucleotide polymorphism, Consanguinity, Biology, Polymorphism, Single Nucleotide, Epithelium, Gene Expression Regulation, Enzymologic, Distal renal tubular acidosis, Internal medicine, Genetics, medicine, Humans, Child, Polymorphism, Single-Stranded Conformational, Genetics (clinical), Genetics & Heredity, LINKAGE ANALYSIS, Genetic heterogeneity, Metabolic acidosis, LOCALIZATION, Acidosis, Renal Tubular, DNA, VPH1P, medicine.disease, GENE, Proton-Translocating ATPases, Endocrinology, Ear, Inner, Mutation, SUBUNIT, ATPASE, Original Article, Female, Sensorineural hearing loss, medicine.symptom, Microsatellite Repeats

وصف الملف: text/plain

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7323617c8b70e848435d24316e3ad062
http://hdl.handle.net/11655/14277

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