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Hematology Volume 23, 2018 - Issue 8
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Hemolytic Anemia

Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I

Prabhakar S. KedarNational Institute of Immunohematology, Indian Council of Medical Research, Mumbai, IndiaCorrespondence[email protected]
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,
Vinod GuptaNational Institute of Immunohematology, Indian Council of Medical Research, Mumbai, IndiaORCID Iconhttp://orcid.org/0000-0002-2400-014XView further author information
ORCID Icon,
Prashant WarangNational Institute of Immunohematology, Indian Council of Medical Research, Mumbai, IndiaView further author information
,
Ashish ChiddarwarNational Institute of Immunohematology, Indian Council of Medical Research, Mumbai, IndiaView further author information
&
Manisha MadkaikarNational Institute of Immunohematology, Indian Council of Medical Research, Mumbai, IndiaView further author information
Pages 567-573 | Published online: 27 Feb 2018

References

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