Search Results - Bittner, Reginald E.

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    Biallelic NSUN3 variants cause diverse phenotypic spectrum disease: from isolated optic atrophy to severe early-onset mitochondrial disorder by Jurkute, Neringa (Author) , Brennenstuhl, Heiko (Author) , Kustermann, Monika (Author) , Van Haute, Lindsey (Author) , Mutti, Christian D. (Author) , Bugiardini, Enrico (Author) , Handa, Takayuki (Author) , Shimura, Masaru (Author) , Petzold, Axel (Author) , Acheson, James (Author) , Robson, Anthony G. (Author) , Macken, William L. (Author) , Hanna, Michael G. (Author) , Pitceathly, Robert D. S. (Author) , Merve, Ashirwad (Author) , Kotzaeridou, Urania (Author) , Kölker, Stefan (Author) , Freilinger, Michael (Author) , Erdler, Marcus (Author) , Bittner, Reginald E. (Author) , Mayr, Johannes A. (Author) , Okazaki, Yasushi (Author) , Murayama, Kei (Author) , Prokisch, Holger (Author) , Webster, Andrew R. (Author) , Minczuk, Michal (Author) , Arno, Gavin (Author) , Pemp, Berthold (Author) , Hoffmann, Georg F. (Author) , Schmidt, Wolfgang M. (Author) , Yu-Wai-Man, Patrick (Author) ,


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