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Publications by Yoshinori Takizawa
Mutation Analysis of the MYO7A and CDH23 Genes in Japanese Patients With Usher Syndrome Type 1
Journal of Human Genetics
Genetics
Erratum To: Increased Phosphatidylcholine (16:0/16:0) in the Folliculus Lymphaticus of Warthin Tumor
Analytical and Bioanalytical Chemistry
Biochemistry
Analytical Chemistry
Related publications
Novel USH2A Mutations in Japanese Usher Syndrome Type 2 Patients: Marked Differences in the Mutation Spectrum Between the Japanese and Other Populations
Journal of Human Genetics
Genetics
Usher Syndrome Type 1 Associated With Primary Ciliary Aplasia
Archives of Ophthalmology
Origin of Vestibular Dysfunction in Usher Syndrome Type 1B
Neurobiology of Disease
Neurology
Mutation Analysis of NPHP6/CEP290 in Patients With Joubert Syndrome and Senior Loken Syndrome
Journal of Medical Genetics
Genetics
Analysis of SCN1A Mutation and Parental Origin in Patients With Dravet Syndrome
Journal of Human Genetics
Genetics
Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome
Journal of Human Genetics
Genetics
Mutation Analysis of UBE3A in Angelman Syndrome Patients
American Journal of Human Genetics
Genetics
Genetic Heterogeneity in Patients With Bartter Syndrome Type 1
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Postural Instability in Subjects With Usher Syndrome
Frontiers in Neurology
Neurology
