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Publications by Mitsuo Motobayashi
Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Nonocclusive Mesenteric Ischemia After Chemotherapy in an Adolescent Patient With a History of Three Allogeneic Hematopoietic Stem Cell Transplantations for Acute Lymphoblastic Leukemia
Pediatrics and Neonatology
Child Health
Pediatrics
Perinatology
Related publications
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
A Novel Mutation in the WFS1gene Identified in a Taiwanese Family With Low-Frequency Hearing Impairment
BMC Medical Genetics
Genetics
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
MERRF/MELAS Overlap Syndrome: A Double Pathogenic Mutation in Mitochondrial tRNA Genes
Journal of Medical Genetics
Genetics
Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family
Acta Ophthalmologica
Medicine
Ophthalmology
Lack of a Modulative Factor in Locus 8p23 in a Finnish Family With Nonsyndromic Sensorineural Hearing Loss Associated With the 1555A>G Mitochondrial DNA Mutation
European Journal of Human Genetics
Genetics
A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family
American Journal of Medical Genetics, Part A
Genetics
A Novel COL4A4 Mutation Identified in a Chinese Family With Thin Basement Membrane Nephropathy
Scientific Reports
Multidisciplinary
