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Comment on: Sideroblastic anemia associated with multisystem mitochondrial disorders: The phenotypic spectrum of PUS1 and COX10 variants and mtDNA deletions needs to be prospectively assessed
Author(s) -
Finsterer Josef
Publication year - 2019
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.27945
Subject(s) - sideroblastic anemia , mitochondrial dna , medicine , phenotype , genetics , mitochondrial disease , anemia , biology , gene
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