スポンサーリンク
Division of Genetics, International Center for Medical Research, Kobe University School of Medicine | 論文
- 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
- DELETION OF TWENTY SEVEN NUCLEOTIDES WITHIN EXON 11 OF THE BAND 3GENE IDENTIFIED IN OVALOCYTOSIS IN LOMBOK ISLAND, INDONESIA
- 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 basis of glucose-6-phosphate dehydrogenase deficiency among Filipinos
- MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS