S-EPMC6439128 - A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant. - OmicsDI

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A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.

ABSTRACT:

SUBMITTER: Devendra R

PROVIDER: S-EPMC6439128 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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