New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1

Serine palmitoyltransferase long chain base subunit 1 (SPTLC1) encodes a serine palmitoyltransferase (SPT) resident in the endoplasmic reticulum (ER). Pathological SPTLC1 variants cause a form of hereditary sensory and autonomic neuropathy (HSAN1A), and have recently been linked to unrestrained sphi...

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Detalles Bibliográficos
Autores principales: Kölbel, Heike, Kraft, Florian, Hentschel, Andreas, Czech, Artur, Gangfuss, Andrea, Mohassel, Payam, Nguyen, Chi, Stenzel, Werner, Schara-Schmidt, Ulrike, Preuße, Corinna, Roos, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140917/
https://www.ncbi.nlm.nih.gov/pubmed/35627278
http://dx.doi.org/10.3390/genes13050893

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140917/
https://www.ncbi.nlm.nih.gov/pubmed/35627278
http://dx.doi.org/10.3390/genes13050893

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