Published in
Elsevier, Molecular and Cellular Probes, 5(29), p. 323-329
DOI: 10.1016/j.mcp.2015.05.012
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Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline
Journal article published in 2015 by
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
and other authors.
,
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
and other authors.
This paper is available in a repository.
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