Genetic basis of neurodevelopmental disorders in 103 Jordanian families
Tawfiq Froukh(Philadelphia University), Rebecca Buchert(Institute of Human Genetics), Beate Kootz(University of Tübingen), Sana' A. S. Al Hait(Jordan Hospital), Moath Hamadallah(The Farah Hospital), Ayman J. Alfrook(Jordan Hospital), Julia Sommerfeld(University of Tübingen), Philipp Alexander Koch(University of Tübingen), Anis Al‐Nazer(Philadelphia University), Lucia Laugwitz(University Children's Hospital Tübingen), Aya Baraghiti(Philadelphia University), Angelika Rieß(University of Tübingen), Johannes Hanselmann(University of Tübingen), Wael Al‐Ameri(Jordan Hospital), Olaf Rieß(STZ eyetrial), Tala Issa(Philadelphia University), Rami Abou Jamra(Leipzig University), Omar Nafie(Mutah University), Marc Sturm(University of Tübingen), Peter Bauer(Centogene (Germany)), Linda Sofan(Philadelphia University), Tobias B. Haack(Technical University of Munich)
Cited by 30
Related Papers
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
|Journal of Medical Genetics|2017|254
Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
|The American Journal of Human Genetics|2014|157
SYT1-associated neurodevelopmental disorder: a case series
|Brain|2018|143