Hasil Pencarian - Saija Ahonen

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  1. 1
    Canine MPV17 truncation without clinical manifestations

    Canine MPV17 truncation without clinical manifestations oleh Reetta L. Hänninen, Saija Ahonen, Merce Màrquez, Maarit J. Myöhänen, Marjo K. Hytönen, Hannes Lohi

    Diterbitkan 2015-10-01
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  2. 2
    Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom

    Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom oleh Saija Ahonen, Ian Seath, Clare Rusbridge, Susan Holt, Gill Key, Travis Wang, Peixiang Wang, Berge A. Minassian

    Diterbitkan 2021-12-01
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  3. 3
    Lafora disease in miniature Wirehaired Dachshunds.

    Lafora disease in miniature Wirehaired Dachshunds. oleh Lindsay Swain, Gill Key, Anna Tauro, Saija Ahonen, Peixiang Wang, Cameron Ackerley, Berge A Minassian, Clare Rusbridge

    Diterbitkan 2017-01-01
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  4. 4
    Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom

    Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom oleh Saija Ahonen, Ian Seath, Clare Rusbridge, Susan Holt, Gill Key, Travis Wang, Peixiang Wang, Berge A. Minassian

    Diterbitkan 2018-03-01
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  5. 5
    Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease

    Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease oleh Maria Kaukonen, Sean Woods, Saija Ahonen, Seppo Lemberg, Maarit Hellman, Marjo K. Hytönen, Perttu Permi, Tom Glaser, Hannes Lohi

    Diterbitkan 2018-05-01
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  6. 6
    A novel form of progressive retinal atrophy in Swedish vallhund dogs.

    A novel form of progressive retinal atrophy in Swedish vallhund dogs. oleh Ann E Cooper, Saija Ahonen, Jessica S Rowlan, Alison Duncan, Eija H Seppälä, Päivi Vanhapelto, Hannes Lohi, András M Komáromy

    Diterbitkan 2014-01-01
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  7. 7
    Canine Lafora Disease: An Unstable Repeat Expansion Disorder

    Canine Lafora Disease: An Unstable Repeat Expansion Disorder oleh Thilo von Klopmann, Saija Ahonen, Irene Espadas-Santiuste, Kaspar Matiasek, Daniel Sanchez-Masian, Stefan Rupp, Helene Vandenberghe, Jeremy Rose, Travis Wang, Peixiang Wang, Berge Arakel Minassian, Clare Rusbridge

    Diterbitkan 2021-07-01
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  8. 8
    An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.

    An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs. oleh Richard Everson, Louise Pettitt, Oliver P Forman, Olivia Dower-Tylee, Bryan McLaughlin, Saija Ahonen, Maria Kaukonen, András M Komáromy, Hannes Lohi, Cathryn S Mellersh, Jane Sansom, Sally L Ricketts

    Diterbitkan 2017-01-01
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  9. 9
    P577: Genetic findings in afor cohort of over 1,800 patients tested with a combined cardiomyopathy and arrhythmia panel*

    P577: Genetic findings in afor cohort of over 1,800 patients tested with a combined cardiomyopathy and arrhythmia panel* oleh Julie Hathaway, Johanna Huusko, Marcos Cicerchia, Saija Ahonen, Johanna Tommiska, Kim Gall, Khalida Liaquat, Victoria Howell, Allison Sluyters, Janica Djupsjöbacka, Mikko Muona, Inka Saarinen, Eija Seppala, Tiia Kangas-Kontio, Lotta Koskinen, Pertteli Salmenperä, Samuel Myllykangas, Juha Koskenvuo

    Diterbitkan 2024-01-01
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  10. 10
    GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

    GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy oleh Krista Heliö, Mikko I. Mäyränpää, Inka Saarinen, Saija Ahonen, Heidi Junnila, Johanna Tommiska, Sini Weckström, Miia Holmström, Mia Toivonen, Kjell Nikus, Kjell Nikus, Julie Hathaway, Pauli Siivonen, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo

    Diterbitkan 2021-11-01
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  11. 11
    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy. oleh Juha W Koskenvuo, Inka Saarinen, Saija Ahonen, Johanna Tommiska, Sini Weckström, Eija H Seppälä, Sari Tuupanen, Tiia Kangas-Kontio, Jennifer Schleit, Krista Heliö, Julie Hathaway, Anders Gummesson, Pia Dahlberg, Tiina H Ojala, Ville Vepsäläinen, Ville Kytölä, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö

    Diterbitkan 2021-01-01
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