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Publications by Katsuhiro Hosono

Mutation Analysis of the MYO7A and CDH23 Genes in Japanese Patients With Usher Syndrome Type 1

Journal of Human Genetics
Genetics
2010English

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
2011English

Usher Syndrome Type 1 Associated With Primary Ciliary Aplasia

Archives of Ophthalmology
2003English

Origin of Vestibular Dysfunction in Usher Syndrome Type 1B

Neurobiology of Disease
Neurology
2001English

Mutation Analysis of NPHP6/CEP290 in Patients With Joubert Syndrome and Senior Loken Syndrome

Journal of Medical Genetics
Genetics
2007English

Analysis of SCN1A Mutation and Parental Origin in Patients With Dravet Syndrome

Journal of Human Genetics
Genetics
2010English

Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

Journal of Human Genetics
Genetics
2000English

Mutation Analysis of UBE3A in Angelman Syndrome Patients

American Journal of Human Genetics
Genetics
1998English

Genetic Heterogeneity in Patients With Bartter Syndrome Type 1

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2016English

Postural Instability in Subjects With Usher Syndrome

Frontiers in Neurology
Neurology
2019English

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