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AP 1S2 ‐truncating variant in a patient with severe neurodevelopmental disorder and cerebral folate deficiency
Author(s) -
Cappuccio Gerarda,
Torella Annalaura,
Mastrangelo Mario,
Carducci Claudia,
Nigro Vincenzo,
BrunettiPierri Nicola,
Leuzzi Vincenzo
Publication year - 2019
Publication title -
acta paediatrica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 115
eISSN - 1651-2227
pISSN - 0803-5253
DOI - 10.1111/apa.14633
Subject(s) - medicine , pediatrics , intellectual disability , psychiatry
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