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Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

  • Sandra Mercier (Lead / Corresponding author)
  • , Sébastien Küry
  • , Emmanuelle Salort-Campana
  • , Armelle Magot
  • , Uchenna Agbim
  • , Thomas Besnard
  • , Nathalie Bodak
  • , Chantal Bou-Hanna
  • , Flora Bréhéret
  • , Perrine Brunelle
  • , Florence Caillon
  • , Brigitte Chabrol
  • , Valérie Cormier-Daire
  • , Albert David
  • , Bruno Eymard
  • , Laurence Faivre
  • , Dominique Figarella-Branger
  • , Emmanuelle Fleurence
  • , Mythily Ganapathi
  • , Romain Gherardi
    • Alice Goldenberg, Antoine Hamel, Jeanine Igual, Alan D. Irvine, Dominique Israël-Biet, Caroline Kannengiesser, Christian Laboisse, Cédric Le Caignec, Jean Yves Mahé, Stéphanie Mallet, Stuart MacGowan, Maeve A. McAleer, Irwin McLean, Cécile Méni, Arnold Munnich, Jean Marie Mussini, Peter L. Nagy, Jeffrey Odel, Grainne M. O'Regan, Yann Péréon, Julie Perrier, Juliette Piard, Eve Puzenat, Jacinda B. Sampson, Frances Smith, Nadem Soufir, Kurenai Tanji, Christel Thauvin, Christina Ulane, Rosemarie M. Watson, Nonhlanhla P. Khumalo, Bongani M. Mayosi, Sébastien Barbarot, Stéphane Bézieau

Research output: Contribution to journal › Article › peer-review

46   Link opens in a new tab Citations (Scopus)
302 Downloads (Pure)

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