Granzow_2015_Mol.Cell.Probes_29_323

Reference

Title : Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline - Granzow_2015_Mol.Cell.Probes_29_323
Author(s) : 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 CR , Bauer P , Moog U
Ref : Mol Cell Probes , 29 :323 , 2015
Abstract : Granzow_2015_Mol.Cell.Probes_29_323
ESTHER : Granzow_2015_Mol.Cell.Probes_29_323
PubMedSearch : Granzow_2015_Mol.Cell.Probes_29_323
PubMedID: 26050939

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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 CR, Bauer P, Moog U (2015)
Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline
Mol Cell Probes 29 :323

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 CR, Bauer P, Moog U (2015)
Mol Cell Probes 29 :323