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Publications by Saara Finnilä
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
Related publications
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
Frequency and Clinical Features of Patients With Sensorineural Hearing Loss Associated With the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics
Journal of Human Genetics
Genetics
Increased Risk of Sensorineural Hearing Loss and Migraine in Patients With a Rare Mitochondrial DNA Variant 4336A>G in tRNAGln
Journal of Medical Genetics
Genetics
Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family
Acta Ophthalmologica
Medicine
Ophthalmology
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
Modiolar Dehiscence Associated With Sensorineural Hearing Loss
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
Neurology
Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
Neurology
Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family
Bioscience Reports
Biochemistry
Cell Biology
Molecular Biology
Biophysics
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
