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Publikováno v:
Nigerian Journal of Paediatrics. 48:50-53
Gangliosidoses belong to the group of genetic lipid metabolism disorders, caused by defects of lysosome enzymes, inherited as an autosomal recessive trait. Gangliosidosis GM1 is caused by the deficiency of the acid beta-galactosidase (GLB11) resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93e65217ca45914d7864b17e75e52aaf
https://doi.org/10.4314/njp.v48i1.10
https://doi.org/10.4314/njp.v48i1.10
