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Comprehensive variant spectrum of theCNGA3gene in patients ..:
Solaki, Maria
;
Baumann, Britta
;
Reuter, Peggy
...
Human Mutation. 43 (2022) 7 - p. 832-858 , 2022
Link:
https://doi.org/10.1002/humu.24371
RT Journal T1
Comprehensive variant spectrum of theCNGA3gene in patients affected by achromatopsia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_humu.24371&Exemplar=1&LAN=DE A1 Solaki, Maria A1 Baumann, Britta A1 Reuter, Peggy A1 Andreasson, Sten A1 Audo, Isabelle A1 Ayuso, Carmen A1 Balousha, Ghassan A1 Benedicenti, Francesco A1 Birch, David A1 Bitoun, Pierre A1 Blain, Delphine A1 Bocquet, Beatrice A1 Branham, Kari A1 Català‐Mora, Jaume A1 De Baere, Elfride A1 Dollfus, Helene A1 Falana, Mohammed A1 Giorda, Roberto A1 Golovleva, Irina A1 Gottlob, Irene A1 Heckenlively, John R. A1 Jacobson, Samuel G. A1 Jones, Kaylie A1 Jägle, Herbert A1 Janecke, Andreas R. A1 Kellner, Ulrich A1 Liskova, Petra A1 Lorenz, Birgit A1 Martorell‐Sampol, Loreto A1 Messias, André PB Hindawi Limited YR 2022 SN 1059-7794 SN 1098-1004 JF Human Mutation VO 43 IS 7 SP 832 OP 858 LK http://dx.doi.org/https://doi.org/10.1002/humu.24371 DO https://doi.org/10.1002/humu.24371 SF ELIB - SuUB Bremen
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