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1 Ergebnisse
1
Deep‐intronic variants inCNGB3cause achromatopsia by pseudo..:
Weisschuh, Nicole
;
Sturm, Marc
;
Baumann, Britta
...
Human Mutation. 41 (2019) 1 - p. 255-264 , 2019
Link:
https://doi.org/10.1002/humu.23920
RT Journal T1
Deep‐intronic variants inCNGB3cause achromatopsia by pseudoexon activation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_humu.23920&Exemplar=1&LAN=DE A1 Weisschuh, Nicole A1 Sturm, Marc A1 Baumann, Britta A1 Audo, Isabelle A1 Ayuso, Carmen A1 Bocquet, Beatrice A1 Branham, Kari A1 Brooks, Brian P. A1 Catalá‐Mora, Jaume A1 Giorda, Roberto A1 Heckenlively, John R. A1 Hufnagel, Robert B. A1 Jacobson, Samuel G. A1 Kellner, Ulrich A1 Kitsiou‐Tzeli, Sofia A1 Matet, Alexandre A1 Martorell Sampol, Loreto A1 Meunier, Isabelle A1 Rudolph, Günther A1 Sharon, Dror A1 Stingl, Katarina A1 Streubel, Berthold A1 Varsányi, Balázs A1 Wissinger, Bernd A1 Kohl, Susanne PB Hindawi Limited YR 2019 SN 1059-7794 SN 1098-1004 JF Human Mutation VO 41 IS 1 SP 255 OP 264 LK http://dx.doi.org/https://doi.org/10.1002/humu.23920 DO https://doi.org/10.1002/humu.23920 SF ELIB - SuUB Bremen
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