An overview of clinical, molecular, and therapeutic approaches to Niemann-Pick disease

In animal cells (especially humans), there is an enzyme called acid sphingomyelinase (ASM) (EC 3.1.4.12) which can break the large molecule of sphingomyelin and convert it into smaller structures of ceramide and phosphorylcholine.

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Journal
Journal of Clinical and Experimental Hematology
Published
2024-08-19
DOI
https://doi.org/10.46439/hematol.3.016
Primary Topic
Lysosomal Storage Disorders Research
Type
article
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article

An overview of clinical, molecular, and therapeutic approaches to Niemann-Pick disease

Kamran Hosseini
Journal of Clinical and Experimental Hematology
Lysosomal Storage Disorders Research
article

An overview of clinical, molecular, and therapeutic approaches to Niemann-Pick disease

Kamran Hosseini
article en

Abstract

In animal cells (especially humans), there is an enzyme called acid sphingomyelinase (ASM) (EC 3.1.4.12) which can break the large molecule of sphingomyelin and convert it into smaller structures of ceramide and phosphorylcholine.

Journal of Clinical and Experimental HematologyVol. 3(1)
Shiraz University of Medical Sciences (IR)
Openalex Percentile: Top 82%
Lysosomal Storage Disorders Research
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An overview of clinical, molecular, and therapeutic approaches to Niemann-Pick disease — Kamran Hosseini · Journal of Clinical and Experimental Hematology (2024) | TGRS Research Map | TGRS