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Autor:
Min-Joon Han, Ida Annunziata, Jason Weesner, Yvan Campos, Muneeb Salie, Carla O'Reilly, Alessandra d'Azzo
Publikováno v:
Stem Cell Research, Vol 46, Iss , Pp 101836- (2020)
Sialidosis is an autosomal recessive lysosomal storage disease, belonging to the glycoproteinoses. The disease is caused by deficiency of the sialic acid-cleaving enzyme, sialidase 1 or neuraminidase 1 (NEU1). Patients with sialidosis are classified
Externí odkaz:
https://doaj.org/article/54b0b88fc04045d5b1ac57709d78fd3a