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1 Ergebnisse
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CNGB1 ‐related rod‐cone dystrophy: A mutation review and up..:
Nassisi, Marco
;
Smirnov, Vasily, M
;
Solis Hernandez, Cyntia
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.24205. , 2021
Link:
https://hal.sorbonne-universite.fr/hal-03240900
RT Journal T1
CNGB1 ‐related rod‐cone dystrophy: A mutation review and update
UL https://suche.suub.uni-bremen.de/peid=base-ftinserm:oai:HAL:hal-03240900v1&Exemplar=1&LAN=DE A1 Nassisi, Marco A1 Smirnov, Vasily, M A1 Solis Hernandez, Cyntia A1 Mohand-Saïd, Saddek A1 Condroyer, Christel A1 Antonio, Aline A1 Kühlewein, Laura A1 Kempf, Melanie A1 Kohl, Susanne A1 Wissinger, Bernd A1 Nasser, Fadi A1 Ragi, Sara, D A1 Wang, Nan-Kai A1 Sparrow, Janet, R A1 Greenstein, Vivienne, C A1 Michalakis, Stylianos A1 Mahroo, Omar, A A1 Ba-Abbad, Rola A1 Michaelides, Michel A1 Webster, Andrew, R A1 Degli Esposti, Simona A1 Saffren, Brooke A1 Capasso, Jenina A1 Levin, Alex A1 Hauswirth, William, W A1 Dhaenens, Claire-Marie A1 Defoort-Dhellemmes, Sabine A1 Tsang, Stephen, H A1 Zrenner, Eberhart A1 Sahel, Jose-Alain A1 Petersen-Jones, Simon A1 Zeitz, Christina A1 Audo, Isabelle PB HAL CCSD; Wiley YR 2021 K1 CNGB1 K1 cyclic nucleotide-gated channel K1 genotype-phenotype correlation K1 inherited retinal disease K1 retinitis pigmentosa K1 rod-cone dystrophy K1 [SDV]Life Sciences [q-bio] JF info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.24205 LK http://dx.doi.org/https://hal.sorbonne-universite.fr/hal-03240900 DO https://hal.sorbonne-universite.fr/hal-03240900 SF ELIB - SuUB Bremen
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