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Scientific Reports
Achondroplasia (ACH), the most common genetic dwarfism in human, is caused by a gain-of function mutation in fibroblast growth factor receptor 3 (FGFR3). Currently, there is no effective treatment for ACH. The development of an appropriate human-rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5e2cbfe57c53680ecba9fefd464c955
https://pubmed.ncbi.nlm.nih.gov/28230213
https://pubmed.ncbi.nlm.nih.gov/28230213
