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Autor:
Maria Vittoria, Masala, S, Scapaticci, Carla, Olivieri, Cesare, Pirodda, Maria Antonietta, Montesu, Maria Antonietta, Cuccuru, Sara, Pruneddu, Cesare, Danesino, Decio, Cerimele
Publikováno v:
European journal of dermatology : EJD. 17(3)
Werner syndrome (WS, MIM#277700) is a very rare autosomal recessive disorder. WS clinical signs include altered distribution of subcutaneous fat, juvenile bilateral cataracts, a mask-like face and bird-like nose, trophic ulcers of the feet, diabetes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8fbd04bfab2e81a405470cff3324ab8
https://pubmed.ncbi.nlm.nih.gov/17478382
https://pubmed.ncbi.nlm.nih.gov/17478382
