Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21-Reference-Cited by-同舟云学术

Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21

Author:

Martinez‐Thompson Jennifer M.¹,Niu Zhiyv²³,Tracy Jennifer A.¹,Moore Steven A.⁴,Swenson Andrea⁵,Wieben Eric D.⁶,Milone Margherita¹

Affiliation:

1. Department of NeurologyMayo Clinic200 First Street SW, Rochester Minnesota55905 USA

2. Department of Laboratory Medicine & PathologyMayo ClinicRochester Minnesota USA

3. Department of Clinical GenomicsMayo ClinicRochester Minnesota USA

4. Department of Pathology University of IowaIowa CityIowa USA

5. Department of NeurologyUniversity of IowaIowa City Iowa USA

6. Department of Biochemistry & Molecular BiologyMayo ClinicRochester Minnesota USA

Funder

Mayo Clinic Center for Individualized Medicine

Department of Neurology, Mayo Clinic

Iowa Wellstone Muscular Dystrophy Cooperative Research Center U54

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

Reference14 articles.

5. Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies;Hauerslev S;BMC Musc Dis,2012

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