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Publikováno v:
HCA Healthc J Med
Description Simpson-Golabi-Behmel syndrome is a rare, X-linked recessive syndrome associated with mutations in the genes encoding glypican 3 (GPC3). The majority of cases have been described in pediatric males, with those affected showing manifestati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2461d705ce29828dae5c011bf71383e
https://europepmc.org/articles/PMC10324786/
https://europepmc.org/articles/PMC10324786/
