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SGCA gene
Known as:
DYSTROGLYCAN 2
, LGMD2D
, DAG2
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National Institutes of Health
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Related topics
Related topics
3 relations
Alpha-Sarcoglycanopathies
SGCB gene
alpha-Sarcoglycan
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Sarcolemmal alpha and gamma sarcoglycan protein deficiencies in Turkish siblings with a novel missense mutation in the alpha sarcoglycan gene.
G. Diniz
,
Hulya Tosun Yildirim
,
+4 authors
A. Tukun
Pediatric Neurology
2014
Corpus ID: 207349253
Highly Cited
1996
Highly Cited
1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
M. Passos-Bueno
,
E. Moreira
,
+10 authors
M. Zatz
Journal of Medical Genetics
1996
Corpus ID: 5099731
Autosomal recessive limb-girdle muscular dystrophies (AR LGMD) represent a group of muscle diseases with a wide spectrum of…
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1996
1996
Developmental expression of dystrophin, dystrophin-associated glycoproteins and other membrane cytoskeletal proteins in human skeletal and heart muscle.
M. Mora
,
C. Di Blasi
,
+4 authors
F. Cornelio
Brain research. Developmental brain research
1996
Corpus ID: 23427049
1996
1996
CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA
M. Salih
,
A H Maluli
,
+4 authors
K. Campbell
Developmental Medicine & Child Neurology
1996
Corpus ID: 16724921
The clinical, biochemical and histochemical features of 14 patients (nine females and five males) with severe childhood autosomal…
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Highly Cited
1995
Highly Cited
1995
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin
Asa Ljunggren
,
David J. Duggan
,
+4 authors
E. Hoffman
Annals of Neurology
1995
Corpus ID: 25249612
In our experience, more than half of muscular dystrophy patients show a primary dystrophinopathy. The underlying cause of…
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1995
1995
Interactions between dystrophin glycoprotein complex proteins.
R. Madhavan
,
H. Jarrett
Biochemistry
1995
Corpus ID: 23678020
The organization of the dystrophin glycoprotein complex (DGC) was studied by investigating interactions between its components…
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Highly Cited
1994
Highly Cited
1994
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
E. McNally
,
M. Yoshida
,
Y. Mizuno
,
E. Ozawa
,
Louis M. Kunkel
Proceedings of the National Academy of Sciences…
1994
Corpus ID: 44892304
Mutations in the dystrophin gene cause the X chromosome-linked, recessive Duchenne and Becker muscular dystrophies. Dystrophin, a…
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1994
1994
Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study
F. Tomé
,
K. Matsumura
,
M. Chevallay
,
K. Campbell
,
M. Fardeau
Neuromuscular Disorders
1994
Corpus ID: 10491870
1994
1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
N. Romero
,
F. Tomé
,
+7 authors
M. Fardeau
Comptes rendus de l'Academie des sciences. Serie…
1994
Corpus ID: 22409786
Severe autosomal recessive muscular dystrophy (SCARMD), McKusick n. 253700, has been originally described in North-African…
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1993
1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
M. Fardeau
,
K. Matsumura
,
+4 authors
K. Campbell
Comptes rendus de l'Academie des sciences. Serie…
1993
Corpus ID: 22510322
A large oligomeric complex of sarcolemmal glycoproteins is associated with dystrophin, the protein absent in Duchenne muscular…
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