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Mutation analysis of SLC37A4 in a patient with glycogen storage disease-type Ib
OBJECTIVE: The aim of the study was to investigate the relationship between SLC37A4 gene mutation and clinical phenotype in a patient with glycogen storage disease-type I. METHODS: The clinical data of one patient with glycogen storage disease-type I accumulation syndrome and the results of SLC37A4...
Guardat en:
| Publicat a: | J Int Med Res |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7045669/ https://ncbi.nlm.nih.gov/pubmed/31617422 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060519867819 |
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