MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS
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概要
- 論文の詳細を見る
- Japan Society of Human Geneticsの論文
- 1997-12-31
著者
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Matsuo Masafumi
Division Of Genetics Icmr Kobe University
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Patria Suryono
Division Of Genetics International Center For Medical Research Kobe University School Of Medicine
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ROMI M.
Division of Genetics, International Center for Medical Research, Kobe University School of Medicine
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Romi M.
Division Of Genetics International Center For Medical Research Kobe University School Of Medicine
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Romi M.Mansyur
Division of Genetics, International Center for Medical Research, Kobe University School of Medicine
関連論文
- Clinical Types, Molecular Genetic Diagnosis & Genetic : clinical Correlation in Patients with Spinal Muscular Atrophy
- Deletion of the SMN1 and NAIP Genes in Vietnamese Patients with Spinal Muscular Atrophy
- Molecular Genetic Analyses of Five Vietnamese Patients with Spinal Musucular Atrophy
- Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
- Molecular Diagnosis, Correlation of Clinical and Deletion Data in Duchenne Muscular Dystrophy
- The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase Deficiency in Vietnam
- DELETION OF TWENTY SEVEN NUCLEOTIDES WITHIN EXON 11 OF THE BAND 3GENE IDENTIFIED IN OVALOCYTOSIS IN LOMBOK ISLAND, INDONESIA
- インドネシア東ジャワ地方の前頭骨篩骨脳瘤患者にMTHFR遺伝子のC677T変異は認められなかった
- A COMPREHENSIVE METHOD TO SCAN FOR POINT MUTATIONS OF THE GLUCOSE 6 PHOSPHATE DEHYDROGENASE GENE
- COMPARISON OF INSERTION RATE OF L1 RETROPOSON INTO INTRON 30 OF THE NEUROFIBROMATOSIS TYPE 1 GENE IN SEVEN ASIAN AND PACIFIC POPULATIONS
- Comparative study on deletions of the dystrophin gene in three Asian populations
- C TO T TRANSITION AT THE FIRST NUCLEOTIDE OF CODON 63 OF THE β-GLOBIN GENE CORRESPONDING TO HEMOGLOBIN M-SASKATOON IN AN INDONESIAN BOY
- Molecular identification and characterization of a novel gene that is upregulated in obese mouse heart
- Screening for glucose-6-phosphate dehydrogenase deficiency using a modified formazan method : A pilot study on Filipino male newborns
- Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase Deficiency in Malays in Malaysia
- A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5
- Molecular genetics of spinal muscular atrophy : contribution of the NAIP gene to clinical severity
- Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient
- Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene : a novel source of genomic instability
- A simple explanation for a case of incompatibility with the reading frame theory in Duchenne muscular dystrophy: failure to detect an aberrant restriction fragment in Southern blot analysis
- Ligand orientation governs conjugation capacity of UDP-glucuronosyltransferase 1A1
- Duchenne/Becker muscular dystrophy:from molecular diagnosis to gene therapy
- Molecular basis of glucose-6-phosphate dehydrogenase deficiency among Filipinos
- MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS
- Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages