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| Home > Publications Database > Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. > print |
| 001 | 155504 | ||
| 005 | 20230915090508.0 | ||
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| 024 | 7 | _ | |a 1018-4813 |2 ISSN |
| 024 | 7 | _ | |a 1476-5438 |2 ISSN |
| 037 | _ | _ | |a DZNE-2021-00700 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a Hengel, Holger |0 P:(DE-2719)2811940 |b 0 |e First author |u dzne |
| 245 | _ | _ | |a Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. |
| 260 | _ | _ | |a Basingstoke |c 2022 |b Stockton Press |
| 336 | 7 | _ | |a article |2 DRIVER |
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| 700 | 1 | _ | |a Buchert, Rebecca |0 0000-0001-7576-3326 |b 1 |
| 700 | 1 | _ | |a Sturm, Marc |b 2 |
| 700 | 1 | _ | |a Haack, Tobias B |b 3 |
| 700 | 1 | _ | |a Schelling, Yvonne |0 P:(DE-2719)2810446 |b 4 |u dzne |
| 700 | 1 | _ | |a Mahajnah, Muhammad |b 5 |
| 700 | 1 | _ | |a Sharkia, Rajech |0 P:(DE-2719)9001176 |b 6 |u dzne |
| 700 | 1 | _ | |a Azem, Abdussalam |b 7 |
| 700 | 1 | _ | |a Balousha, Ghassan |b 8 |
| 700 | 1 | _ | |a Ghanem, Zaid |b 9 |
| 700 | 1 | _ | |a Falana, Mohammed |0 0000-0002-5893-8945 |b 10 |
| 700 | 1 | _ | |a Balousha, Osama |b 11 |
| 700 | 1 | _ | |a Ayesh, Suhail |b 12 |
| 700 | 1 | _ | |a Keimer, Reinhard |b 13 |
| 700 | 1 | _ | |a Deigendesch, Werner |b 14 |
| 700 | 1 | _ | |a Zaidan, Jimmy |b 15 |
| 700 | 1 | _ | |a Marzouqa, Hiyam |b 16 |
| 700 | 1 | _ | |a Bauer, Peter |0 0000-0001-9414-4555 |b 17 |
| 700 | 1 | _ | |a Schöls, Ludger |0 P:(DE-2719)2810795 |b 18 |e Last author |u dzne |
| 773 | _ | _ | |a 10.1038/s41431-021-00909-7 |0 PERI:(DE-600)2005160-8 |n 2 |p 248 |t European journal of human genetics |v 30 |y 2022 |x 1476-5438 |
| 787 | 0 | _ | |a Hengel, Holger et.al. |d Basingstoke : Stockton Press, 2020 |i RelatedTo |0 DZNE-2020-01287 |r |t First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. |
| 856 | 4 | _ | |y OpenAccess |u https://pub.dzne.de/record/155504/files/DZNE-2021-00700.pdf |
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