Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Huseyin Cizer"'
Autor:
Aimee Donald, Huseyin Cizer, Niamh Finnegan, Tanya Collin-Histed, Derralynn A. Hughes, Elin Haf Davies
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Gaucher disease is an inherited lysosomal storage disorder of which there are three subtypes. Type 1 disease has no neurological involvement and is treatable with enzyme replacement therapy. Type 2 disease results in infant death
Externí odkaz:
https://doaj.org/article/21c54a1db1534c9087dfd23b1a72e4b2
Autor:
Elin Haf Davies, Huseyin Cizer, Niamh Finnegan, Tanya Collin-Histed, Derralynn Hughes, Aimee Donald
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Background Gaucher disease is an inherited lysosomal storage disorder of which there are three subtypes. Type 1 disease has no neurological involvement and is treatable with enzyme replacement therapy. Type 2 disease results in infant death and type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f9a6bb0fd02a9ddaee7006e84d0cf9
http://europepmc.org/articles/PMC6727397
http://europepmc.org/articles/PMC6727397