Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population

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概要

• 論文の詳細を見る
• Springer-Verlag Tokyoの論文
• 2006-04-01

著者

• Epplen Jorg

  Human Genetics Ma5/39 Ruhr-university

• WIECZOREK Stefan

  Human Genetics, MA5/39, Ruhr-University

• ARNING Larissa

  Human Genetics, MA5/39, Ruhr-University

• ALHEITE Ingrid

  Human Genetics, MA5/39, Ruhr-University

• Arning Larissa

  Human Genetics Ma5/39 Ruhr-university

• Wieczorek Stefan

  Human Genetics Ma5/39 Ruhr-university

• Alheite Ingrid

  Human Genetics Ma5/39 Ruhr-university

関連論文

• Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population
• Genetic variations in the genes encoding receptor activator nuclear factor κ B (RANK), receptor activator nuclear factor κ B ligand (RANKL) and osteoprotegerin (OPG) in patients with psoriasis and psoriatic arthritis : A case-control study

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