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Functional analysis of GALT variants found in classic galactosemia patients using a novel cell‐free translation method
Classic galactosemia is an autosomal recessive disorder caused by deleterious variants in the galactose‐1‐phosphate uridylyltransferase (GALT) gene. GALT enzyme deficiency leads to an increase in the levels of galactose and its metabolites in the blood causing neurodevelopmental and other clinical c...
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| Pubblicato in: | JIMD Rep |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley & Sons, Inc.
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6606980/ https://ncbi.nlm.nih.gov/pubmed/31392114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12037 |
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