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pro vyhledávání: '"Nattaya Nutsathapana"'
Publikováno v:
Medical Science and Discovery. 8:289-290
Basal cell nevus syndrome is a rare inherited autosomal dominant syndrome characterized by developmental defects and tumor predisposition. There are more than 400 reported PTCH1 mutations, including frameshift, nonsense, missense, deletions, duplicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::028e9a3866499ee1fcf2216d571635ed
https://doi.org/10.36472/msd.v8i4.519
https://doi.org/10.36472/msd.v8i4.519
