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pro vyhledávání: '"Boris B.T. Wang"'
Publikováno v:
Molecular Genetics and Metabolism. 63:263-269
Galactosemia is a clinically heterogeneous autosomal recessive inborn error of metabolism caused by deficiency of galactose-1-phosphate uridylyltransferase (GALT). Despite the numerous point mutations identified in the GALT gene, the prevalence of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8536618f6c1797e34e3fd9a753b5a3c8
https://doi.org/10.1006/mgme.1998.2678
https://doi.org/10.1006/mgme.1998.2678
