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| 001 | 162809 | ||
| 005 | 20240722111328.0 | ||
| 024 | 7 | _ | |a 10.1038/s41431-021-00935-5 |2 doi |
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| 100 | 1 | _ | |a Schüle-Freyer, Rebecca |0 P:(DE-2719)2812018 |b 0 |e First author |u dzne |
| 245 | _ | _ | |a Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint. |
| 260 | _ | _ | |a Basingstoke |c 2021 |b Stockton Press |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1721639584_12032 |2 PUB:(DE-HGF) |x Erratum/Correction |
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| 773 | _ | _ | |a 10.1038/s41431-021-00935-5 |g Vol. 29, no. 9, p. 1462 - 1465 |0 PERI:(DE-600)2005160-8 |n 9 |p 1462 - 1465 |t European journal of human genetics |v 29 |y 2021 |x 1476-5438 |
| 787 | 0 | _ | |a Schüle-Freyer, Rebecca et.al. |d Basingstoke : Stockton Press, 2021 |i RelatedTo |0 DZNE-2021-00744 |r |t Solving unsolved rare neurological diseases-a Solve-RD viewpoint. |
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