Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline
Granzow, M., Paramasivam, N., Hinderhofer, K., Fischer, C., Chotewutmontri, S., Kaufmann, L., Evers, C., Kotzaeridou, U., Rohrschneider, K., Schlesner, M., Sturm, M., Pinkert, S., Eils, R., Bartram, CLanguage:
english
Journal:
Molecular and Cellular Probes
DOI:
10.1016/j.mcp.2015.05.012
Date:
June, 2015
File:
PDF, 615 KB
english, 2015