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Uridine treatment normalizes the congenital dyserythropoietic anemia type II ‐like hematological phenotype in a patient with homozygous mutation in the CAD gene
Author(s) -
Russo Roberta,
Marra Roberta,
Andolfo Immacolata,
Manna Francesco,
De Rosa Gianluca,
Rosato Barbara Eleni,
Radhakrishnan Kottayam,
Fahey Michael,
Iolascon Achille
Publication year - 2020
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.25946
Subject(s) - medicine , pediatrics , epilepsy , complete blood count , status epilepticus , cortical blindness , levetiracetam , autism , cobalamin , gastroenterology , psychiatry , optometry , blindness , vitamin b12
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