Biallelic loss of function variants in <i>PPP1R21</i> cause a neurodevelopmental syndrome with impaired endocytic function
Atteeq U. Rehman(Baylor College of Medicine), Miriam Schmidts(University Medical Center Freiburg), Sebastian J. Arnold(University of Freiburg), GholamReza Karami Madani(Damghan University), Zeineb Bakey(Radboud University Nijmegen), Fan Xia(Baylor College of Medicine), Christopher M. Richmond(Victorian Clinical Genetics Services), Francesco Vetrini(Indiana University School of Medicine), Fatma Al Jasmi(United Arab Emirates University), Lihadh Al‐Gazali(United Arab Emirates University), Marios Kambouris(Qatar Airways (Qatar)), Mari Tokita(Baylor College of Medicine), Magdalena Walkiewicz(National Institute of Allergy and Infectious Diseases), Zornitza Stark(Zoos Victoria), Kaman Wu(Radboud University Nijmegen), Hatem El‐Shanti(University of Iowa), Ehsan Ghayoor Karimiani(St George's, University of London), Abolfazl Rad(Sabzevar University of Medical Sciences), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Jozef Hertecant(Tawam Hospital), Federico Santoni(University of Geneva), Stylianos E. Antonarakis(University of Geneva), Jill V. Hunter(Baylor College of Medicine), Martin Helmstädter(University of Freiburg), Periklis Makrythanasis(University of Geneva), Pengfei Liu(Macau University of Science and Technology), Yaping Yang(Jiangsu University), Anna Rajab(Ministry of Health), Maryam Najafi(Radboud University Nijmegen), Christine M. Eng(Baylor College of Medicine), Weimin He(Baylor College of Medicine), Andrea Petersen(Legacy Emanuel Medical Center), Hanan Hamamy(University of Geneva), Sebastian Lunke(Royal Children's Hospital)
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