Hasil Pencarian - Paulina Bahena

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  1. 1
    A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family

    A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family oleh Julia Doll, Michaela A. H. Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, Barbara Vona

    Diterbitkan 2020-08-01
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  2. 2
    Expanding the clinical phenotype of IARS2-related mitochondrial disease

    Expanding the clinical phenotype of IARS2-related mitochondrial disease oleh Barbara Vona, Reza Maroofian, Emanuele Bellacchio, Maryam Najafi, Kyle Thompson, Ahmad Alahmad, Langping He, Najmeh Ahangari, Abolfazl Rad, Sima Shahrokhzadeh, Paulina Bahena, Falk Mittag, Frank Traub, Jebrail Movaffagh, Nafise Amiri, Mohammad Doosti, Reza Boostani, Ebrahim Shirzadeh, Thomas Haaf, Daria Diodato, Miriam Schmidts, Robert W. Taylor, Ehsan Ghayoor Karimiani

    Diterbitkan 2018-11-01
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