Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations

Hereditary spastic paraplegia 56 (SPG56) is an extremely rare autosomal recessive disorder caused by mutations in the CYP2U1 gene, involved in fatty acid metabolism. SPG56 causes progressive spasticity in upper and lower limbs, though due to the rarity of this subtype of spastic paraplegia, the mole...

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Bibliografiske detaljer

Principais autores:	Hannah C. Leeson, Denise Goh, David Coman, Ernst J. Wolvetang
Format:	Artigo
Sprog:	Inglês
Udgivet:	Elsevier 2022-10-01
Serier:	Stem Cell Research
Online adgang:	http://www.sciencedirect.com/science/article/pii/S1873506122002665
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