AP1S2 -truncating variant in a patient with...

Acta Paediatrica 2018 / 11

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

Cappuccio, Gerarda, Torella, Annalaura, Mastrangelo, Mario, Carducci, Claudia, Nigro, Vincenzo, Brunetti-Pierri, Nicola, Leuzzi, Vincenzo
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Language:
english
Journal:
Acta Paediatrica
DOI:
10.1111/apa.14633
Date:
November, 2018
File:
PDF, 648 KB
english, 2018
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