Back to Results
First PageMeta Content
Cytoskeleton / Proteins / Dystrophin / Dystrobrevin / Syntrophin / Syncoilin / Utrophin / Sarcoglycan / Dysbindin / Biology / Muscular dystrophy / Anatomy


Neuromuscular Disorders[removed]–467 www.elsevier.com/locate/nmd Deficiency of the syntrophins and a-dystrobrevin in patients with inherited myopathy K.J. Jonesa,b, A.G. Comptona,b, N. Yanga, M.A. Millsa, M.F. Pet
Add to Reading List

Document Date: 2007-10-24 04:00:13

Open Document

File Size: 4,43 MB

Share Result on Facebook

City

Boston / Westgrove / Pittsburgh / /

Company

Elsevier Science B.V. / GenBank / Olympus / Millipore / Amersham / Astra Zeneca Pharmaceuticals / Jackson ImmunoResearch Laboratories Inc. / Bio-Rad / /

Country

United States / Australia / United Kingdom / Monaco / /

Currency

GBP / /

/

Facility

Sydney Children’s Hospital / University of Sydney / Children’s Hospital / The Children’s Hospital / University of Washington / /

IndustryTerm

protein product / Cerebral imaging / length product / /

MedicalCondition

mild muscular dystrophy / Neuromuscular Disorders / Muscular dystrophy / congenital heart disease / human skeletal muscle disease / Myopathy / inherited myopathy K.J. Jonesa / muscle weakness / congenital myopathy / CMD / limb-girdle muscular dystrophy / severe hypotonia / skeletal muscle weakness / human muscle disease / e.g. myotonic dystrophy / dystrobrevin deficiency / myopathies / merosin-deficient congenital muscular dystrophy / inflammatory myopathy / spinal muscular atrophy / fibre necrosis / marked hypotonia / disease / extraocular muscle weakness / NMJ dysfunction / autosomal recessive muscular dystrophy / Duchenne muscular dystrophy / marked deficiency / muscle disease exhibiting abnormalities / pulmonary artery stenosis / neonatal period Congenital myopathy / variable deficiency / muscle disease / muscular dystrophies / mitochondrial myopathy / hypotonia / congenital muscular dystrophy / Deficiency / contractures / complete external ophthalmoplegia / congenital-onset hypotonia / congenital muscular dystrophies / genetically determined disorders / /

Organization

Harvard Medical School / Division of Genetics / National Institute of Health / University of Sydney / Sydney / Sydney Children’s Hospital / Department of Physiology and Biophysics / Children’s Hospital / Institute for Neuromuscular Research / Department of Paediatrics and Child Health / Muscular Dystrophy Association of NSW / DAPC / University of Washington / Seattle / Howard Hughes Medical Institute / /

Person

Ana Domazetovska / Daniel MacArthur / Harriet Lo / Ben Othmane / /

/

Position

Corresponding author / /

ProvinceOrState

New Hampshire / /

Technology

alpha / antibodies / cloning / Digital Imaging / gel electrophoresis / /

URL

www.elsevier.com/locate/nmd / /

SocialTag