A missense mutation in a patient with guanosine triphosphate cyclohydrolase I deficiency missed in the newborn screening program
- 31 March 1995
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 126 (3) , 401-405
- https://doi.org/10.1016/s0022-3476(95)70458-2
Abstract
No abstract availableKeywords
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