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Indexed/Abstracted in: CAB, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 0,532
Online ISSN 1827-1715
Gragnani S. G., Michelotti F., Rocca R., Sardi R., Bardini N.
A case of primary congenital lymphedema is reported. Asymmetrical involvement of the low limbs and unremarcable family history for lymphedema (indicating of de novo mutation) was the main findings.
language: English, Italian