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A Novel GCH1 Mutation in An Indian Child with GTP Cyclohydrolase Deficiency

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References

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VKR: Revised and approved the manuscript for important intellectual content and will act as guarantor of the paper; BN: Diagnosis, management and writing the manuscript; VMS: Conducted laboratory tests and analyzed the data; AB: Conducted laboratory tests and revision of the manuscript.

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Correspondence to Vykuntaraju K. Gowda.

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Gowda, V.K., Nagarajan, B., Srinivasan, V.M. et al. A Novel GCH1 Mutation in An Indian Child with GTP Cyclohydrolase Deficiency. Indian J Pediatr 86, 752–753 (2019). https://doi.org/10.1007/s12098-019-02900-z

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  • DOI: https://doi.org/10.1007/s12098-019-02900-z

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