Expanding the Phenotype of GTF2E2‐associated Trichothiodystrophy
JEADV Journal of the European Academy of Dermatology and Venereology/Journal of the European Academy of Dermatology and Venereology(2023)
摘要
Journal of the European Academy of Dermatology and VenereologyAccepted Articles LETTER TO THE EDITOR Expanding the phenotype of GTF2E2-associated trichothiodystrophy Brian Sperelakis-Beedham, Corresponding Author Brian Sperelakis-Beedham [email protected] orcid.org/0000-0003-2828-460X Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France Correspondence Dr. Brian Sperelakis-Beedham, Robert-Debré University Hospital, 48 Bd Sérurier, 75019 Paris, France. Email address: Email: [email protected]Search for more papers by this authorLyse Ruaud, Lyse Ruaud Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorYoann Vial, Yoann Vial orcid.org/0000-0003-1437-0427 Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorMyriam Rachid, Myriam Rachid Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Neuroscience Department, Human Genetics and Cognitive Function Unit, Pasteur Institute, Paris, FranceSearch for more papers by this authorFaustine Ageorges, Faustine Ageorges Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorLouise Goujon, Louise Goujon Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorAlain Verloes, Alain Verloes Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorAnne-Claude Tabet, Anne-Claude Tabet Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France Neuroscience Department, Human Genetics and Cognitive Function Unit, Pasteur Institute, Paris, FranceSearch for more papers by this authorEmmanuelle Bourrat, Emmanuelle Bourrat Department of Dermatology, Hôpital Saint Louis, AP-HP, Paris, France These authors contributed equally to this paperSearch for more papers by this authorJonathan Lévy, Jonathan Lévy Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France These authors contributed equally to this paperSearch for more papers by this author Brian Sperelakis-Beedham, Corresponding Author Brian Sperelakis-Beedham [email protected] orcid.org/0000-0003-2828-460X Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France Correspondence Dr. Brian Sperelakis-Beedham, Robert-Debré University Hospital, 48 Bd Sérurier, 75019 Paris, France. Email address: Email: [email protected]Search for more papers by this authorLyse Ruaud, Lyse Ruaud Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorYoann Vial, Yoann Vial orcid.org/0000-0003-1437-0427 Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorMyriam Rachid, Myriam Rachid Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Neuroscience Department, Human Genetics and Cognitive Function Unit, Pasteur Institute, Paris, FranceSearch for more papers by this authorFaustine Ageorges, Faustine Ageorges Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorLouise Goujon, Louise Goujon Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorAlain Verloes, Alain Verloes Genetics Department, APHP, Robert-Debré University Hospital, Paris, FranceSearch for more papers by this authorAnne-Claude Tabet, Anne-Claude Tabet Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France Neuroscience Department, Human Genetics and Cognitive Function Unit, Pasteur Institute, Paris, FranceSearch for more papers by this authorEmmanuelle Bourrat, Emmanuelle Bourrat Department of Dermatology, Hôpital Saint Louis, AP-HP, Paris, France These authors contributed equally to this paperSearch for more papers by this authorJonathan Lévy, Jonathan Lévy Genetics Department, APHP, Robert-Debré University Hospital, Paris, France Plateforme SeqOIA, AP-HP, Paris, France These authors contributed equally to this paperSearch for more papers by this author First published: 04 October 2023 https://doi.org/10.1111/jdv.19545 This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. 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