Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Alicia Giner-Ayala"'
Publikováno v:
Journal of Clinical and Scientific Research, Vol 10, Iss 4, Pp 197-201 (2021)
Background: Niemann-Pick disease type B is an autosomal recessive lysosomal storage disorder caused by a deficiency of acid sphingomyelinase (ASM) coded by SMPD1 gene. Diagnostic assays for this enzyme were developed using fibroblasts, leukocytes, pl
Externí odkaz:
https://doaj.org/article/c529f8b8c75e49ff97bcd6c0072bc248
