Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum
Véronique Pingault(Hôpital Necker-Enfants Malades), Jeanne Amiel(Hôpital Necker-Enfants Malades), Berta Campos(Oryzon Genomics (Spain)), Houda Zghal Elloumi, C. Neiva-Vaz(Hôpital Necker-Enfants Malades), Núria Martínez‐Gil(Vall d'Hebron Institut de Recerca), Esther Nibbeling(University Medical Center Groningen), Alanna Strong(Children's Hospital of Philadelphia), Arnaud Picard(Hôpital Necker-Enfants Malades), Amaia Lasa‐Aranzasti(Vall d'Hebron Institut de Recerca), Judite de Oliveira(Hôpital Necker-Enfants Malades), Pierre Blanc, Radka Stoeva(Centre Hospitalier du Mans), Françoise Ochsenbein(Centre National de la Recherche Scientifique), Tabib Dabir(Belfast Health and Social Care Trust), Sylvain Hanein(Inserm), Parul Jayakar(Miami Children's Hospital), Inge M. M. Lakeman(Leiden University Medical Center)
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