- Article
Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
- Ilaria Bestetti,
- Milena Crippa,
- Alessandra Sironi,
- Francesca Tumiatti,
- Maura Masciadri,
- Marie Falkenberg Smeland,
- Swati Naik,
- Oliver Murch,
- Maria Teresa Bonati and
- Alice Spano
- + 17 authors
KBG syndrome (KBGS) is a neurodevelopmental disorder caused by the Ankyrin Repeat Domain 11 (ANKRD11) haploinsufficiency. Here, we report the molecular investigations performed on a cohort of 33 individuals with KBGS clinical suspicion. By using a mu...