Presence of three mutations in the fumarylacetoacetate...

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Molecular Genetics and Metabolism 2019 / 2

Presence of three mutations in the fumarylacetoacetate hydrolase gene in a patient with atypical symptoms of hereditary tyrosinemia type I

Morrow, Geneviève, Dreumont, Natacha, Bourrelle-Langlois, Maxime, Roy, Vincent, Tanguay, Robert M.
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Language:
english
Journal:
Molecular Genetics and Metabolism
DOI:
10.1016/j.ymgme.2019.01.019
Date:
February, 2019
File:
PDF, 947 KB
english, 2019
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