Search Results - Glöckle, Nicola

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    Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation by Weik, Anja Kathrin (Author) , Rohrschneider, Klaus (Author) , Strom, Tim M. (Author) , Glöckle, Nicola (Author) , Kohl, Susanne (Author) , Wissinger, Bernd (Author) , Weisschuh, Nicole (Author) ,


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