Ehlers-Danlos syndrome in two siblings with deficient lysyl hydroxylase activity in cultured skin fibroblasts but only mild hydroxylysine deficit in skin.
Year: 1975
Type: article
Study design: Case Report
Source: PubMed
Authors: B Steinmann, R Gitzelmann, A Vogel, M E Grant, R Harwood, C H Sear
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2416638018