Stephanie C Crosson
Overview
Explore the profile of Stephanie C Crosson including associated specialties, affiliations and a list of published articles.
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2
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73
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Recent Articles
1.
Reinhard J, Lin S, McKee K, Meinen S, Crosson S, Sury M, et al.
Sci Transl Med
. 2017 Jun;
9(396).
PMID: 28659438
-related muscular dystrophy ( MD or MDC1A) is the most frequent form of early-onset, fatal congenital muscular dystrophies. It is caused by mutations in , the gene encoding laminin-α2, the...
2.
McKee K, Crosson S, Meinen S, Reinhard J, Ruegg M, Yurchenco P
J Clin Invest
. 2017 Feb;
127(3):1075-1089.
PMID: 28218617
Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous mutation in Lama2 (dy2J mice) express a nonpolymerizing...