AP1S2 ‐truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency

Acta Paediatrica,Volume 0, Issue ja, -Not available-.

Source: Acta Paediatrica - November 1, 2018 Category: Pediatrics Authors: Gerarda Cappuccio, Annalaura Torella, Mario Mastrangelo, Claudia Carducci, Vincenzo Nigro, Nicola Brunetti ‐Pierri, Vincenzo Leuzzi Source Type: research