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4. Expanding the genetic and phenotypic spectrum of branched‐chain amino acid transferase 2 deficiency. Issue 5 (1st August 2019)

6. Nonketotic hyperglycinemia: Functional assessment of missense variants in GLDC to understand phenotypes of the disease. Issue 6 (20th March 2017)

7. On the 'Disclosure Initiative – Principles of Disclosure': The EAA Financial Reporting Standards Committee's View. (2nd January 2020)

8. Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia. Issue 7 (30th April 2020)