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Description
Mutations in the GCH1 gene are the cause of the autosomal recessive disorder referred to as HPABH4B
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Exp Hematol 27:489495
7 out of 8 RCTs (742 infants), reported growth data at 36 months corrected age and 2 reported neurodevelopmental outcomes at 612 months, and will be further discussed later in this chapter (306, 312)
