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Paper Details

<i>ALPK3</i> gene mutation in a patient with congenital cardiomyopathy and dysmorphic features.
Cold Spring Harb Mol Case Stud
19
2017
ALPK3, ALPK3 gene, Gln675SerfsX30, Primary cardiomyopathy, c.2018delC, cardiac abnormalities, cardiomyopathy, congenital cardiomyopathy, disease-causing genes, dysmorphic features, genetic disorders, hypertrophic cardiomyopathy, infant, inherited cardiac diseases, patient, primary dilated cardiomyopathy
Author NameAffiliation
Ahmet Okay CaglayanIstanbul Bilim University
Ahmet Okay CaglayanYale School of Medicine
Akdes Serin HarmanciYale School of Medicine
Mark W YoungbloodYale School of Medicine
Kaya BilguvarYale Center for Genome Analysis, Yale School of Medicine
Murat GunelYale School of Medicine
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Release 1.2