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Original research
Improving the clinical interpretation of missense variants in X linked genes using structural analysis

Authors

  • Shalaw Rassul Sallah Division of Evolution and Genomic Sciences, The University of Manchester Faculty of Biology, Medicine and Health, Manchester, UKManchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre, Manchester, UK PubMed articlesGoogle scholar articles
  • Jamie M Ellingford Division of Evolution and Genomic Sciences, The University of Manchester Faculty of Biology, Medicine and Health, Manchester, UKManchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre, Manchester, UK PubMed articlesGoogle scholar articles
  • Panagiotis I Sergouniotis Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre, Manchester, UK PubMed articlesGoogle scholar articles
  • Simon C Ramsden Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre, Manchester, UK PubMed articlesGoogle scholar articles
  • Nicholas Lench Congenica Ltd, Biodata Innovation Centre, Wellcome Genome Campus, Hinxton, London, UK PubMed articlesGoogle scholar articles
  • Simon C Lovell Division of Evolution and Genomic Sciences, The University of Manchester Faculty of Biology, Medicine and Health, Manchester, UK PubMed articlesGoogle scholar articles
  • Graeme C Black Division of Evolution and Genomic Sciences, The University of Manchester Faculty of Biology, Medicine and Health, Manchester, UKManchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre, Manchester, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Graeme C Black; graeme.black{at}manchester.ac.uk
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Citation

Sallah SR, Ellingford JM, Sergouniotis PI, et al
Improving the clinical interpretation of missense variants in X linked genes using structural analysis

Publication history

  • Received August 19, 2020
  • Revised January 18, 2021
  • Accepted January 21, 2021
  • First published March 25, 2021.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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