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  1. 1
    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access

    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access von Jones, Amy V, Curtiss, Darin, Harris, Claire, Southerington, Tom, Hautalahti, Marco, Wihuri, Pauli, Mäkelä, Johanna, Kallionpää, Roosa E, Makkonen, Enni, Knopp, Theresa, Mannermaa, Arto, Mäkinen, Erna, Moilanen, Anne-Mari, Tezel, Tongalp H, Waheed, Nadia K

    Veröffentlicht in PloS one

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  2. 2
    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access

    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access von Jones, Amy V, Cu, Harris, Claire, Southerington, Tom, Hautalahti, Marco, Wihuri, Pauli, Mäkelä, Johanna, Kallionpää, Roosa E, Makkonen, Enni, Knopp, Theresa, Mannermaa, Arto, Mäkinen, Erna, Moilanen, Anne-Mari, Tezel, Tongalp H, Waheed, Nadia K

    Veröffentlicht in PLoS ONE

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  3. 3
    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access

    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access von Jones, Amy V, Curtiss, Darin, Harris, Claire, Southerington, Tom, Hautalahti, Marco, Wihuri, Pauli, Mäkelä, Johanna, Kallionpää, Roosa E, Makkonen, Enni, Knopp, Theresa, Mannermaa, Arto, Mäkinen, Erna, Moilanen, Anne-Mari, Tezel, Tongalp H, Waheed, Nadia K

    Veröffentlicht in PLoS ONE

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  4. 4
    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access

    An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access von Jones, Amy V, Curtiss, Darin, Harris, Claire, Southerington, Tom, Hautalahti, Marco, Wihuri, Pauli, Mäkelä, Johanna, Kallionpää, Roosa E, Makkonen, Enni, Knopp, Theresa, Mannermaa, Arto, Mäkinen, Erna, Moilanen, Anne-Mari, Tezel, Tongalp H, Waheed, Nadia K

    Veröffentlicht in PLoS ONE

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