Hotta Y | Department Of Pharmacology Aichi Medical University

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著作論文

CLINICAL FEATURES OF JAPANESE LEBER'S HEREDITARY OPTIC NEUROPATHY WITH 11778 MUTATION OF MITOCHONDRIAL DNA
Multicenter Genetic Study of Retinitis Pigmentosa in Japan : II. Prevalence of Autosomal Recessive Retinitis Pigmentosa
MISSENSE MUTATION OF RHODOPSIN GENE CODON 15 FOUND IN JAPANESE AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
Long-term Follow-up of Two Sisters with Leber's Hereditary Optic Neuropathy
Analysis of Peripherin/RDS Gene for Japanese Retinal Dystrophies
FREQUENCIES OF POLYMORPHISMS IN THE RHODOPSIN GENE OF JAPANESE RETINITIS PIGMENTOSA AND NORMAL INDIVIDUALS
Studies on Cardiac Ingredients of Plants. XIII : Chemical Modification of Gitoxin to Cardiotonic Compounds without Vascular Contractile Effect
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778
Arg124Cys Mutation of the βig-h3 Gene in a Japanese Family With Lattice Corneal Dystrophy Type I
Central Corneal Thickness in Japanese Children
DNA Analysis for Diagnosis of X-Linked Juvenile Retinoschisis When Clinical Examination Is Difficult in a Young Child
CLONING AND HIGH EXPRESSION OF RABBIT FKBP25 IN CORNEA
Case of a Japanese Patient with X-linked Ocular Albinism Associated with the GPR143 Gene Mutation
Novel USH2A mutations in Japanese Usher syndrome type 2 patients : marked differences in the mutation spectrum between the Japanese and other populations
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes

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