Generation of FOUR iPSC lines (CRICKi004-A; CRICKi005-A; CRICKi006-A, CRICKi007-A) from Spinal muscle atrophy patients with lower extremity dominant (SMALED) phenotype

Spinal muscular atrophy with lower extremity dominant (SMALED) is a hereditary neuromuscular disorder characterized by degeneration of spinal cord motor neurons resulting in lower limbs muscle weakness and paralysis. Mutations in DYNC1H1, which encodes BICD2, a multifunctional adaptor for microtubul...

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Bibliographic Details

Published in:	Stem Cell Research
Main Authors:	Liani G. Devito, Fay Cooper, Ilenia D'Angelo, Jim Smith, Lyn Healy
Format:	Article
Language:	English
Published:	Elsevier 2022-12-01
Online Access:	http://www.sciencedirect.com/science/article/pii/S1873506122003038