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Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1mutation: phenotypic variations ranging from late presentation to spontaneous resolution

Authors :
Brandt, Agnieszka
Agarwal, Neha
Giri, Dinesh
Yung, Zoe
Didi, Mohammad
Senniappan, Senthil
Source :
Journal of Pediatric Endocrinology & Metabolism; May 2020, Vol. 33 Issue: 5 p675-679, 5p
Publication Year :
2020

Details

Language :
English
ISSN :
0334018X and 21910251
Volume :
33
Issue :
5
Database :
Supplemental Index
Journal :
Journal of Pediatric Endocrinology & Metabolism
Publication Type :
Periodical
Accession number :
ejs53131289
Full Text :
https://doi.org/10.1515/jpem-2019-0416