OSCR

Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomaly.

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Code

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johnwmillr/Facer

License: MIT
State: the link answers
Copies: kept by the registry: this license allows it
Tools found in the code: Matplotlib, NumPy, OpenCV

Overview

Authors: Quentin Thomas, Marialetizia Motta, Thierry Gautier, Maha S Zaki, Andrea Ciolfi, Julien Paccaud, François Girodon, Odile Boespflug-Tanguy, Thomas Besnard, Jennifer Kerkhof, Haley McConkey, Aymeric Masson, Anne-Sophie Denommé-Pichon, Benjamin Cogné, Eva Trochu, Virginie Vignard, Fatima El It, Lance H Rodan, Mohammad Ayman Alkhateeb, Rami Abou Jamra
and 43 other authorsLaurence Duplomb, Emilie Tisserant, Yannis Duffourd, Ange-Line Bruel, Adam Jackson, Siddharth Banka, Meriel McEntagart, Anand Saggar, Joseph G Gleeson, David Sievert, Hyunwoo Bae, Beom Hee Lee, Kisang Kwon, Go Hun Seo, Hane Lee, Anjum Saeed, Nadeem Anjum, Huma Cheema, Salem Alawbathani, Imran Khan, Jorge Pinto-Basto, Joyce Teoh, Jasmine Wong, Umar Bin Mohamad Sahari, Henry Houlden, Kristina Zhelcheska, Melanie Pannetier, Mona A Awad, Marion Lesieur-Sebellin, Giulia Barcia, Jeanne Amiel, Julian Delanne, Christophe Philippe, Laurence Faivre, Sylvie Odent, Aida Bertoli-Avella, Christel Thauvin, Bekim Sadikovic, Bruno Reversade, Reza Maroofian, Jérôme Govin, Marco Tartaglia, Antonio Vitobello
Published: 30 August 2022
Type: Brief report
Status: code verified (how the code is found and verified)
License: CC BY
Institutions: Inserm (France), Université de Bourgogne (France), Université Bourgogne Franche-Comté (France), Centre de recherche Translationnelle en Médecine moléculaire (France), Bambino Gesù Children's Hospital (Italy), Centre National de la Recherche Scientifique (France), Institut pour l'avancée des biosciences (France), Université Grenoble Alpes (France), Armed Forces College of Medicine (Egypt), National Research Centre (Egypt), CHU Dijon Bourgogne (France), Université Paris Cité (France), Assistance Publique – Hôpitaux de Paris (France), Hôpital Robert-Debré (France), NeuroDiderot (France), Centre Hospitalier Universitaire de Nantes (France), Institut du Thorax (France), Université de Nantes (France), Nantes Université (France), London Health Sciences Centre (Canada), Western University (Canada), Boston Children's Hospital (United States), Harvard University (United States), Hamad Medical Corporation (Qatar), University Hospital Leipzig (Germany), University of Manchester (United Kingdom), St Mary's Hospital (United Kingdom), Manchester University NHS Foundation Trust (United Kingdom), Health Innovation Manchester (United Kingdom), St George’s University Hospitals NHS Foundation Trust (United Kingdom), The Portland Hospital (United Kingdom), University of California San Diego (United States), Rady Children's Institute for Genomic Medicine (United States), Asan Medical Center (South Korea), University of Ulsan (South Korea), 3billion, Inc. (South Korea) (South Korea), University of Child Health Sciences (Pakistan), Centogene (Germany) (Germany), Agency for Science, Technology and Research (Singapore), Genome Institute of Singapore (Singapore), National Hospital for Neurology and Neurosurgery (United Kingdom), UCL Queen Square Institute of Neurology (United Kingdom), University College London (United Kingdom), Centre Hospitalier Universitaire de Rennes (France), Hôpital Necker-Enfants Malades (France), Institut de génétique et de développement de Rennes (France), Université de Rennes (France), Koç University (Türkiye), King Abdullah University of Science and Technology (Saudi Arabia)

Data

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