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The spastic paraplegia-associated phospholipase DDHD1 is a primary brain phosphatidylinositol lipase
Deleterious mutations in the serine hydrolase DDHD1 cause the SPG28 subtype of the neurological disease Hereditary Spastic Paraplegia (HSP), which is characterized by axonal neuropathy and gait impairments. DDHD1 has been shown to display PLA1-type phospholipase activity with a preference for phosph...
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| Publicado no: | Biochemistry |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6237197/ https://ncbi.nlm.nih.gov/pubmed/30221923 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.biochem.8b00810 |
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