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Functional characterization of the first missense variant i..:
Ascari, Giulia
;
Peelman, Frank
;
Farinelli, Pietro
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187288/. , 2020
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187288/
RT Journal T1
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
UL https://suche.suub.uni-bremen.de/peid=base-ftpubmed:oai:pubmedcentral.nih.gov:7187288&Exemplar=1&LAN=DE A1 Ascari, Giulia A1 Peelman, Frank A1 Farinelli, Pietro A1 Rosseel, Toon A1 Lambrechts, Nina A1 Wunderlich, Kirsten A A1 Wagner, Matias A1 Nikopoulos, Konstantinos A1 Martens, Pernille A1 Balikova, Irina A1 Derycke, Lara A1 Holtappels, Gabriële A1 Krysko, Olga A1 Van Laethem, Thalia A1 De Jaegere, Sarah A1 Guillemyn, Brecht A1 De Rycke, Riet A1 De Bleecker, Jan A1 Creytens, David A1 Van Dorpe, Jo A1 Gerris, Jan A1 Bachert, Claus A1 Neuhofer, Christiane A1 Walraedt, Sophie A1 Bischoff, Almut A1 Pedersen, Lotte B A1 Klopstock, Thomas A1 Rivolta, Carlo A1 Leroy, Bart P A1 De Baere, Elfride A1 Coppieters, Frauke PB John Wiley and Sons Inc. YR 2020 K1 Research Articles JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187288/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187288/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187288/ SF ELIB - SuUB Bremen
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