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pro vyhledávání: '"Isabelle Schrouff"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Stuve-Wiedemann syndrome (SWS) is a rare and severe genetic disease characterized by skeletal anomalies and dysautonomic disturbances requiring appropriate care. Peer support is mandatory to fill the lack of clinical recommendatio
Externí odkaz:
https://doaj.org/article/39d78c0919794538b2152385aa3f8bc7
