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Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics

        Correction to: Genetics in Medicine 2022; https://doi.org/10.1038/gim.2017.84
        In the article “Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics” by Strovel ET et al (Genet Med 2017;19:P1-10), there was an error in Figure 1. The labels "Acetyl-CoA carboxylase E.C. 6.4.1.2” and “Pyruvate carboxylase E.C. 6.4.1.1” were placed incorrectly at the bottom of the figure artwork. See revised Figure 1 shown on next page.

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        • Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics
          Genetics in MedicineVol. 19Issue 10
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            Disclaimer: These ACMG Standards and Guidelines are intended as an educational resource for clinical laboratory geneticists to help them provide quality clinical laboratory genetic services. Adherence to these Standards and Guidelines is voluntary and does not necessarily assure a successful medical outcome. These Standards and Guidelines should not be considered inclusive of all proper procedures and tests or exclusive of others that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, clinical laboratory geneticists should apply their professional judgment to the specific circumstances presented by the patient or specimen.
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