Molecular and clinical spectra of FBXL4 deficiency
Year: 2017
Type: article
Study design: Observational Study
Source: Human Mutation
DOI: 10.1002/humu.23341
Authors: Ayman W. El-Hattab, Hongzheng Dai, Mohammed Almannai, Julia Wang, Eissa A. Faqeih, Ali Al Asmari, Mohammed A. M. Saleh, Mohammed A. O. Elamin, Majid Alfadhel, Fowzan S. Alkuraya, Mais Hashem, Mazhor S. Aldosary, Rawan Almass, Faten B. Almutairi, Maysoon Alsagob, Mohammed Al-Owain, Shirin Al-Sharfa, Zuhair N. Al-Hassnan, Zuhair Rahbeeni, Mohammed A. Al-Muhaizea, Nawal Makhseed, Gretchen K. Foskett, David A. Stevenson, Natalia Gomez-Ospina, Chung Lee, Richard G. Boles, Samantha A. Schrier Vergano, Saskia B. Wortmann, Wolfgang Sperl, Thomas Opladen, Georg F. Hoffmann, Maja Hempel, Holger Prokisch, Bader Alhaddad, Johannes A. Mayr, Wenyaw Chan, Namik Kaya, Lee-Jun C. Wong
Institutions: Tawam Hospital, Baylor College of Medicine, King Fahd Medical City, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, King Abdullah International Medical Research Center, National Guard Health Affairs, Alfaisal University, King Faisal Specialist Hospital & Research Centre, Jahra Hospital, Ministry of Health, Stanford Medicine, Stanford University, Children's Hospital of The King's Daughters, Paracelsus Medical University, Helmholtz Munich, Salzburger Landeskliniken, Institut für Humangenetik, Technical University of Munich, University Hospital Heidelberg, University Medical Center Hamburg-Eppendorf, The University of Texas Health Science Center at Houston
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
Award: G1838092687
OpenAlex ID: W2757541068