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A Compound Heterozygous Mutation in Calpain 1 Identifies a ..:
G. Perez-Siles
;
M. Ellis
;
A. Ashe
...
https://www.frontiersin.org/articles/10.3389/fgene.2021.801253/full. , 2022
Link:
https://doi.org/10.3389/fgene.2021.801253
RT Journal T1 <Title>A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4)</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:6324a42e1da947ec8f90dabe93e5418e&Exemplar=1&LAN=DE A1 G. Perez-Siles A1 M. Ellis A1 A. Ashe A1 B. Grosz A1 S. Vucic A1 M. C. Kiernan A1 K. A. Morris A1 S. W. Reddel A1 M. L. Kennerson PB Frontiers Media S.A. YR 2022 K1 spinal muscular atrophy K1 calpain K1 patient fibroblasts K1 non-SMN1 K1 β-catenin K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2021.801253/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2021.801253 DO https://doi.org/10.3389/fgene.2021.801253 SF ELIB - SuUB Bremen
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