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Publikováno v:
Laboratory Medicine. 54:327-332
Monogenetic diabetes mellitus (DM) describes a collection of single-gene diseases marked by hyperglycemia presenting in childhood or adulthood and the absence of immunological markers of type 1 DM. Mutations in the human insulin gene INS give rise to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40bcb10771e36fed8d2391858c5498f8
https://doi.org/10.1093/labmed/lmac115
https://doi.org/10.1093/labmed/lmac115
