日本人のSMN1遺伝子上にC117T多型を見出した
スポンサーリンク
概要
- 論文の詳細を見る
- 2007-02-01
著者
-
MATSUO Masafumi
Department of Pediatrics, Graduate School of Medicine, Kobe University
-
NISHIO Hisahide
Department of Genetic Epidemiology, Graduate School of Medicine, Kobe University
-
Matsuo M
Department Of Pediatrics Graduate School Of Medicine Kobe University
-
サデワ アフマド・ハミム
Department Of Public Health Kobe University Graduate School Of Medicine
-
Sadewa Ahmad
神戸大学 大学院医学系研究科小児
-
Harada Y
Department Of Public Health Kobe University Graduate School Of Medicine
-
Harada Yosuke
神戸大学 医系研究小児科
-
Harada Yosuke
Department Of Public Health Kobe University Graduate School Of Medicine
-
Hamim Ahmad
Department Of Environmental Health And Safety Faculty Of Medicine Kobe University Graduate School Of
-
Matsuo Masafumi
Department Of Pediatrics Graduate School Of Medicine Kobe University
-
SASONGKO Teguh
Department of Public Health, Kobe University Graduate School of Medicine
-
Nishio Hisahide
Department Of Genetic Epidemiology Graduate School Of Medicine Kobe University
-
Nishio Hisahide
Department Of Pubic Health And Genetic Epidemiology Kobe University Graduate School Of Medicine
-
Nishio Hisahide
Department Of Environmental Medicine Kobe University
-
Matsuo M
Division Of Genetics International Center For Medical Research Kobe University School Of Medicine
-
Sasongko Teguh
Department Of Pubic Health And Genetic Epidemiology Kobe University Graduate School Of Medicine
-
Nishio H
Department Of Public Health Kobe University Graduate School Of Medicine
-
Mizutori Masakazu
Department Of Pediatrics Graduate School Of Medicine Kobe University
-
サソンコ T.
マレーシア
-
Harada Yosuke
Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Japan
-
NISHIO Hisahide
Department of Community Medicine and Social Healthcare Science, Kobe University Graduate School of Medicine
-
MATSUO Masafumi
Department of Medical Rehabilitation, Faculty of Rehabilitation, Kobegakuin University
-
HARADA Yosuke
Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences
関連論文
- Novel Mutations in 21 Patients with Tuberous Sclerosis Complex and Variation of Tandem Splice-acceptor Sites in TSC1 exon 14
- ベトナム人脊髄性筋萎縮症患者におけるSMN2遺伝子量ならびにNAIP遺伝子量について
- 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
- 全国調査における典型的溶血性尿毒症症候群の重症化因子の検討
- Association of Cumulative Cyclosporine Dose with Its Irreversible Nephrotoxicity in Japanese Patients with Pediatric-Onset Autoimmune Diseases(Biopharmacy)
- 志賀毒素を介さず発症した溶血性尿毒症症候群5症例の予後と腎組織像に関する検討
- A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism
- 小児SLE患者に対する高用量ミゾリビン投与の試み