A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family.

[1 ] Institute for Maternal and Child Health - IRCCS 'Burlo Garofolo', Trieste, Italy.

[2 ] Department of Oral and Maxillofacial Diseases, University of Helsinki, Institute of Dentistry, Helsinki University Central Hospital, Helsinki, Finland.

[3 ] Department of Eye and Vision Science, University of Liverpool, Institute of Ageing and Chronic Disease, Liverpool, UK.

[4 ] Department of Pediatric Dentistry, Faculty of Dentistry, Dicle University, Diyarbakir, Turkey.

[5 ] Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.

[6 ] Medical Genetics Section, Department of Clinical Pathophysiology, University of Florence, Florence, Italy.

[7 ] Medical Genetics Unit, Meyer Children's University Hospital, Florence, Italy.

[8 ] Fondazione IRCCS Cà Granda - Ospedale Maggiore Policlinico Milano, Milan, Italy.

[9 ] Department of Pediatric Dermatology, University of Milan, Milan, Italy.

[10 ] Bambino Gesù Children's Hospital IRCCS, Research Laboratory, Rome, Italy.