Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy

Laminin-α2 related Congenital Muscular Dystrophy (LAMA2-CMD) is a progressive muscle disease caused by partial or complete deficiency of laminin-211, a skeletal muscle extracellular matrix protein. In the last decade, basic science research has queried underlying disease mechanisms in existing LAMA2...

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Vydáno v:J Neuromuscul Dis
Hlavní autoři: Willmann, Raffaella, Gordish-Dressman, Heather, Meinen, Sarina, Rüegg, Markus A., Yu, Qing, Nagaraju, Kanneboyina, Kumar, Ayar, Girgenrath, Mahasweta, Coffey, Caroline B.M., Cruz, Vivian, Van Ry, Pam M., Bogdanik, Laurent, Lutz, Cathleen, Rutkowski, Anne, Burkin, Dean J.
Médium: Artigo
Jazyk:Inglês
Vydáno: IOS Press 2017
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Review
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5467719/
https://ncbi.nlm.nih.gov/pubmed/28550268
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JND-170217
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