Publications by authors named "Katie Styren"

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Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease.
Marisa W Friederich, Abdallah F Elias, Alice Kuster, Lucia Laugwitz, Austin A Larson, Katie Styren

J Inherit Metab Dis· September 2020

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Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome.
John P Johnson, Linda Beischel, Corbin Schwanke, Katie Styren, Amy Crunk

J Assist Reprod Genet· June 2018

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Two microcephaly-associated novel missense mutations in CASK specifically disrupt the CASK-neurexin interaction.
Leslie E W LaConte, Vrushali Chavan, Abdallah F Elias, Cynthia Hudson, Corbin Schwanke, Katie Styren

Hum Genet· March 2018

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