Publications by authors named "Manar M Samman"

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A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes.
Nicole M Fisher, Aqeela AlHashim, Aditi B Buch, Hana Badivuku, Manar M Samman

JCI Insight· February 2021

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Further delineation of METTL23-associated intellectual disability.
Mohammed Almannai, Osama Obaid, Eissa Faqeih, Ali Alasmari, Manar M Samman

Am J Med Genet A· April 2020

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A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder.
Hanan E Shamseldin, Ali Alasmari, Mohammed A Salih, Manar M Samman, Shahid A Mian

Brain· November 2017

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