Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Stefanie V. Heinrich"'
Autor:
Lauren M. Chunn, Jeffrey Bissonnette, Stefanie V. Heinrich, Stephanie A. Mercurio, Mark J. Kiel, Frank Rutsch, Carlos R. Ferreira
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background ENPP1 Deficiency—caused by biallelic variants in ENPP1—leads to widespread arterial calcification in early life (Generalized Arterial Calcification of Infancy, GACI) or hypophosphatemic rickets in later life (Autosomal Recessi
Externí odkaz:
https://doaj.org/article/cd8c2685876a4e608d9abc0c70fac25e
Autor:
Chunn, Lauren M.1 (AUTHOR), Bissonnette, Jeffrey1 (AUTHOR), Heinrich, Stefanie V.1 (AUTHOR), Mercurio, Stephanie A.1 (AUTHOR), Kiel, Mark J.1 (AUTHOR) kiel@genomenon.com, Rutsch, Frank2 (AUTHOR), Ferreira, Carlos R.3 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 12/2/2022, Vol. 17 Issue 1, p1-8. 8p.