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Publications by Hideki Mutai
Variants Encoding a Restricted Carboxy-Terminal Domain of SLC12A2 Cause Hereditary Hearing Loss in Humans
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
TMC and EVER Genes Belong to a Larger Novel Family, the TMC Gene Family Encoding Transmembrane Proteins
BMC Genomics
Biotechnology
Genetics
Related publications
Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss
Laryngoscope
Otorhinolaryngology
Loss-Of-Function Variants in Endothelial Lipase Are a Cause of Elevated HDL Cholesterol in Humans
Journal of Clinical Investigation
Medicine
Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
Journal of Human Genetics
Genetics
Hereditary Bilateral Sudden Sensorineural Hearing Loss
Bratislava Medical Journal
Genotype-Phenotype Correlation in Hereditary Hearing Loss
Gene Therapy for Hereditary Hearing Loss
Congenital Cytomegalovirus Infection: A Cause of Sensorineural Hearing Loss.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
American Journal of Human Genetics
Genetics
Labyrinthine Window Rupture as a Cause of Acute Sensorineural Hearing Loss
European Archives of Oto-Rhino-Laryngology
Medicine
Otorhinolaryngology