SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy

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概要

• 論文の詳細を見る
• Wiley-Blackwellの論文

著者

• 李 明鎭

  神戸大学大学院 医学系研究科 公衆衛生学分野

• Hong Dang

  Institute Of Biotechnology Vietnamese Academy Of Science And Technology

• Myeong Jin

  Department Of Genetic Epidemiology Graduate School Of Medicine Kobe University

• Nishio Hisahide

  Department Of Genetic Epidemiology Graduate School Of Medicine Kobe University

• Lee Myeong

  神戸大学 医学研究科遺伝疫学

• Myeong Jin

  Department Of Pediatrics Kobe University Graduate School Of Medicine

• Teguh Haryo

  Department Of Genetic Epidemiology Graduate School Of Medicine Kobe University

• Nishio H

  Department Of Public Health Kobe University Graduate School Of Medicine

• Lee Myeong　jin

  Department Of Public Health Kobe University Graduate School Of Medicine

• Yamasaki Takemi

  Hyogo Prefectural Children's Hospital

• Takeshima Y

  Hyogo Prefectural Children's Hospital

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
• カドミウム暴露によるホメオボックス遺伝子の発現変動
• 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
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