Miyamura Yoshinori | Department Of Dermatology Nagoya University Graduate School Of Medicine

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著作論文

Investigation of the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome
Characterization of the human RAB38 and RAB7 genes : exclusion of new major pathological loci for Japanese OCA
Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations
A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1)
Polymorphic sequences of the tyrosinase gene : allele analysis on 16 OCA1 patients in Japan indicate that three polymorphic sequences in the tyrosinase gene promoter could be powerful markers for indirect gene diagnosis
Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9
Oculocutaneous Albinism and Analysis of Tyrosinase Gene in Japanese Patients

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