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Anzahl der Publikationen: 2
Zeitschriftenartikel
Peymani, Fatemeh; Ebihara, Tomohiro; Smirnov, Dmitrii; Kopajtich, Robert; Ando, Masahiro; Bertini, Enrico 
ORCID: https://orcid.org/0000-0001-9276-4590; Carrozzo, Rosalba ORCID: https://orcid.org/0000-0002-3327-4054; Diodato, Daria; Distelmaier, Felix ORCID: https://orcid.org/0000-0001-8460-3738; Fang, Fang; Ghezzi, Daniele ORCID: https://orcid.org/0000-0002-6564-3766; Hempel, Maja; Iwanicka-Pronicka, Katarzyna; Klopstock, Thomas ORCID: https://orcid.org/0000-0003-2805-4652; Stenton, Sarah L.; Lamperti, Costanza; Liu, Zhimei; Murtazina, Aysylu; Okamoto, Yuji; Okazaki, Yasushi; Piekutowska-Abramczuk, Dorota; Rötig, Agnés ORCID: https://orcid.org/0000-0003-0589-0703; Ryzhkova, Oxana; Schlein, Christian; Shagina, Olga; Takashima, Hiroshi; Tsygankova, Polina G.; Zech, Michael; Meitinger, Thomas; Shimura, Masaru; Murayama, Kei ORCID: https://orcid.org/0000-0002-3923-8636 und Prokisch, Holger ORCID: https://orcid.org/0000-0003-2379-6286
(2025):
Pleiotropic effects of MORC2 derive from its epigenetic signature.
In: Brain, awaf159 [Forthcoming]
ORCID: https://orcid.org/0000-0001-9276-4590; Carrozzo, Rosalba ORCID: https://orcid.org/0000-0002-3327-4054; Diodato, Daria; Distelmaier, Felix ORCID: https://orcid.org/0000-0001-8460-3738; Fang, Fang; Ghezzi, Daniele ORCID: https://orcid.org/0000-0002-6564-3766; Hempel, Maja; Iwanicka-Pronicka, Katarzyna; Klopstock, Thomas ORCID: https://orcid.org/0000-0003-2805-4652; Stenton, Sarah L.; Lamperti, Costanza; Liu, Zhimei; Murtazina, Aysylu; Okamoto, Yuji; Okazaki, Yasushi; Piekutowska-Abramczuk, Dorota; Rötig, Agnés ORCID: https://orcid.org/0000-0003-0589-0703; Ryzhkova, Oxana; Schlein, Christian; Shagina, Olga; Takashima, Hiroshi; Tsygankova, Polina G.; Zech, Michael; Meitinger, Thomas; Shimura, Masaru; Murayama, Kei ORCID: https://orcid.org/0000-0002-3923-8636 und Prokisch, Holger ORCID: https://orcid.org/0000-0003-2379-6286
(2025):
Pleiotropic effects of MORC2 derive from its epigenetic signature.
In: Brain, awaf159 [Forthcoming]
Stenton, Sarah L.; Tesarova, Marketa; Sheremet, Natalia L.; Catarino, Claudia; Carelli, Valerio; Ciara, Elzbieta; Curry, Kathryn; Engvall, Martin; Fleming, Leah R.; Freisinger, Peter; Iwanicka-Pronicka, Katarzyna; Jurkiewicz, Elzbieta; Klopstock, Thomas; Koenig, Mary K.; Kolarova, Hana; Kousal, Bohdan; Krylova, Tatiana; La Morgia, Chiara; Noskova, Lenka; Piekutowska-Abramczuk, Dorota; Russo, Sam N.; Stranecky, Viktor; Tothova, Iveta; Traisk, Frank und Prokisch, Holger
(2022):
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome.
In: Brain, Bd. 145, Nr. 5: S. 1624-1631
[PDF, 848kB]