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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