Variants in GHR and related pathways may help provide context for individual receptor sensitivity and baseline GH capacity, supporting more informed provider conversations about secretagogue suitability
10.1016/j.ebiom.2018.01.012 EBioMedicine 37 JinY.LuS
Also, if I am a homozygous carrier of the MTHFR mutation (C677T), are my kids definitely carriers of at least one mutation
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