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pro vyhledávání: '"Maria-Anna M.A. D'Souza"'
Publikováno v:
Dermatologic clinics. 28(1)
Kindler syndrome is caused by genetic defects in the focal contact-associated protein, fermitin family homologue 1 (FFH1), encoded by the gene FERMT1 (known as KIND1). Defects in FFH1 lead to abnormal integrin activation and loss of keratinocyte epid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b81146f4f398e6d7ecee28c488c8cc
https://pubmed.ncbi.nlm.nih.gov/19945623
https://pubmed.ncbi.nlm.nih.gov/19945623
