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SGCA gene

Known as: DYSTROGLYCAN 2, LGMD2D, DAG2 
National Institutes of Health

Related topics

Related topics

3 relations
Alpha-SarcoglycanopathiesSGCB genealpha-Sarcoglycan

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1996
1996
CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA
The clinical, biochemical and histochemical features of 14 patients (nine females and five males) with severe childhood autosomal… 
1996
1996
Ultrastructural localization of adhalin in normal murine skeletal myofiber
The ultrastructural localization of adhalin and its relations to dystrophin, β‐dystroglycan, and β‐spectrin were studied in… 
1996
1996
Clinical heterogeneity of adhalin deficiency
We report adhalin deficiency in 8 patients with clinically diagnosed muscular dystrophy, dystrophic histopathological features… 
1996
1996
Electron microscopic observations of triple immunogold labelling for dystrophin, β-dystroglycan and adhalin in human skeletal myofibers
Abstract Dystrophin is the Duchenne muscular dystrophy gene product and is a membrane cytoskeletal protein present in the network… 
1996
1996
Neurosensory hearing loss in secondary adhalinopathy.
We report mild-to-moderate neurosensory hearing loss and severe childhood autosomal recessive muscular dystrophy with adhalin… 
1995
1995
Interactions between dystrophin glycoprotein complex proteins.
The organization of the dystrophin glycoprotein complex (DGC) was studied by investigating interactions between its components… 
Review
1995
Review
1995
[Severe childhood autosomal recessive muscular dystrophy].
Dystrophin is associated with several novel sarcolemmal proteins via the cysteine-rich/C-terminal domains. The dystrophin… 
1995
1995
Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster
1994
1994
Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study
1994
1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
Severe autosomal recessive muscular dystrophy (SCARMD), McKusick n. 253700, has been originally described in North-African… 
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