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Author/Creator Krate, Jonida

1. Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1. (August 2020)

Authors:
Szelinger, Szabolcs; Krate, Jonida; Ramsey, Keri; Strom, Samuel P.; Shieh, Perry B.; Lee, Hane; Belnap, Newell; Balak, Chris; Siniard, Ashley L.; Russell, Megan; Richholt, Ryan; Both, Matt De; Claasen, Ana M.; Schrauwen, Isabelle; Nelson, Stanley F.; Huentelman, Matthew J.; Craig, David W.; Yang,...
Journal:
Neurology
Issue:
Volume 6:Number 4(2020)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Whole transcriptome profiling of the human hippocampus suggests an involvement of the KIBRA rs17070145 polymorphism in differential activation of the MAPK signaling pathway. Issue 7 (22nd April 2017)

Authors:
Piras, Ignazio S; Krate, Jonida; Schrauwen, Isabelle; Corneveaux, Jason J; Serrano, Geidy E; Sue, Lucia; Beach, Thomas G; Huentelman, Matthew J
Journal:
Hippocampus
Issue:
Volume 27:Issue 7(2017)
Page Start:
784
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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