Whole-genome sequencing of patients with rare diseases in a national health system
Most patients with rare diseases do not receive a molecular diagnosis and the aetiological variants and causative genes for more than half such disorders remain to be discovered. Here we used whole-genome sequencing (WGS) in a national health system to streamline diagnosis and to discover unknown ae...
| Hlavní autoři: | , , , , , , , , |
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| Další autoři: | |
| Médium: | Journal article |
| Jazyk: | English |
| Vydáno: |
Springer Nature
2020
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