A NOVEL SEQUENCE POLYMORPHISM IN EXON 8 OF THE HUMAN VITAMIN D-BINDING PROTEIN (GC) GENE IN AN AFRICAN POPULATION
スポンサーリンク
概要
- 論文の詳細を見る
- Japan Society of Human Geneticsの論文
- 1995-03-31
著者
-
Yuasa Isao
Department of Legal Medicine, Tottori University School of Medicine
-
Yuasa Isao
Department Of Legal Medicine Tottori University School Of Medicine
-
Yuasa Isao
Department Of Legal Medicine Faculty Of Medicine Tottori University
-
KOFLER Andrea
Institute of Anthropology and Human Genetics, University of Munich
-
BRAUN Andreas
Institute of Anthropology and Human Genetics, University of Munich
-
BICHLMAIER Regina
Institute of Anthropology and Human Genetics, University of Munich
-
KAMMERER Stefan
Institute of Anthropology and Human Genetics, University of Munich
-
CLEVE Hartwig
Institute of Anthropology and Human Genetics, University of Munich
-
Kammerer Stefan
Institute Of Anthropology And Human Genetics University Of Munich
-
Braun Andreas
Institute Of Anthropology And Human Genetics University Of Munich
-
Cleve Hartwig
Institute Of Anthropology And Human Genetics University Of Munich
-
Kofler Andrea
Institute Of Anthropology And Human Genetics University Of Munich
-
Bichlmaier Regina
Institute Of Anthropology And Human Genetics University Of Munich
関連論文
- The Genotypes of IL-1 beta and MMP-3 are Associated with the Prognosis of HCV-related Hepatocellular Carcinoma
- Molecular characterization of four alpha-l-antitrypsin variant alleles found in Japanese population : a mutation hot spot at the codon for amino acid 362
- Characterization of genomic rearrangements of the α_1-acid glycoprotein/orosomucoid gene in Ghanaians
- A new single-nucleotide polymorphism in the seventh component of complement (C7) gene
- Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
- Carbohydrate-deficient glycoprotein syndrome : electrophoretic study of multiple serum glycoproteins
- ITIH1^* Q0_, A NULL ALLELE OF INTER-ALPHA-TRYPSIN INHIBITOR H1 CAUSED BY DELETION/FRAMESHIFT MUTATION
- Y-chromosomal STR haplotyping in a Japanese population
- A NOVEL SEQUENCE POLYMORPHISM IN EXON 8 OF THE HUMAN VITAMIN D-BINDING PROTEIN (GC) GENE IN AN AFRICAN POPULATION
- Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I
- Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia
- Increased expression of β-hexosaminidase α chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I
- Characterization of an Acidic Polysaccharide Isolated from the Leaves of Corchorus olitorius (Moroheiya)
- Transferrin Polymorphism in the Nansei Islands : Description of a New Variant TF Dama and Clines of Allele Frequencies in Japanese Populations
- A novel 56-bp variable tandem repeat polymorphism in the human deoxyribonuclease I gene and its population data