Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: lessons of the bioinformatics pipeline
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
October 2015
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| In: |
Molecular and cellular probes
Year: 2015, Jahrgang: 29, Heft: 5, Pages: 323-329 |
| ISSN: | 1096-1194 |
| DOI: | 10.1016/j.mcp.2015.05.012 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1016/j.mcp.2015.05.012
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| Verfasserangaben: | M. Granzow, N. Paramasivam, K. Hinderhofer, C. Fischer, S. Chotewutmontri, L. Kaufmann, C. Evers, U. Kotzaeridou, K. Rohrschneider, M. Schlesner, M. Sturm, S. Pinkert, R. Eils, C.R. Bartram, P. Bauer, U. Moog |
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