Validation of dye-binding/high-resolution thermal denaturation for the identification of mutations in theSLC22A5 gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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4. Increased detection of primary carnitine deficiency through second-tier newborn genetic screening;Orphanet Journal of Rare Diseases;2021-03-23
5. Screening 3.4 million newborns for primary carnitine deficiency in Zhejiang Province, China;Clinica Chimica Acta;2020-08
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