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Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH‐cytochrome b5 reductase gene mutations
Author(s) -
Kedar Prabhakar S.,
Warang Prashant,
Ghosh Kanjaksha,
Colah Roshan B.
Publication year - 2011
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.21956
Subject(s) - compound heterozygosity , methemoglobinemia , reductase , genetics , medicine , gene , mutation , biology , biochemistry , enzyme , anesthesia
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