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Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa
Digital博士論文障害者向け資料あり
立花, 信貴MDPI (Multidisciplinary Digital Publishing Institute)2022-02-16
National Diet Library
  • Subject Heading...inal dystrophy congenital disorders of glycosylation SRD5A3 gene RP1-related retin...
  • Note (General)...s suspected of congenital disorders of glycosylation (CDG). We obtained clinical c...

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa
Digital博士論文
立花, 信貴MDPI (Multidisciplinary Digital Publishing Institute)2022-02-16Genes13 2p.359-
Available onlineOther Libraries in Japan
  • Summary, etc....s suspected of congenital disorders of glycosylation (CDG). We obtained clinical c...
  • Subject Heading...inal dystrophy congenital disorders of glycosylation SRD5A3 gene RP1-related retin...

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