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SOX10: 20 years of phenotypic plurality and current understanding of its developmental function

Authors

  • Veronique Pingault Department of Embryology and Genetics of Malformations, INSERM UMR 1163, Université de Paris and Institut Imagine, Paris, FranceService de Génétique des Maladies Rares, AP-HP, Hopital Necker-Enfants Malades, Paris, France PubMed articlesGoogle scholar articles
  • Lisa Zerad Department of Embryology and Genetics of Malformations, INSERM UMR 1163, Université de Paris and Institut Imagine, Paris, France PubMed articlesGoogle scholar articles
  • William Bertani-Torres Department of Embryology and Genetics of Malformations, INSERM UMR 1163, Université de Paris and Institut Imagine, Paris, France PubMed articlesGoogle scholar articles
  • Nadege Bondurand Department of Embryology and Genetics of Malformations, INSERM UMR 1163, Université de Paris and Institut Imagine, Paris, France PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Veronique Pingault, embryology and genetics of malformations, Institut Imagine Institut des Maladies Genetiques, Paris, France; veronique.pingault{at}inserm.fr; Dr Nadege Bondurand; nadege.bondurand{at}inserm.fr
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Citation

Pingault V, Zerad L, Bertani-Torres W, et al
SOX10: 20 years of phenotypic plurality and current understanding of its developmental function

Publication history

  • Received July 21, 2021
  • Accepted September 19, 2021
  • First published October 19, 2021.

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  • 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.

  • 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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