Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bönnemann, MR Passos-Bueno… - Human molecular …, 1996 - academic.oup.com
Autosomal recessive limb-girdle muscular dystrophies (LGMDs) are genetically
heterogeneous. A subgroup of these disorders is caused by mutations in the dystrophin …
被引用次数：154 相关文章

[引用][C] Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bonnemann, MR Passos-Bueno… - Human Molecular …, 1996 - elibrary.ru
[PDF] researchgate.net

[PDF][PDF] Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bönnemann, MR Passos-Bueno… - Human Molecular …, 1996 - researchgate.net
Limb-girdle muscular dystrophies (LGMDs) are a genetically heterogeneous group of
disorders, characterized clinically by predominantly proximal muscle weakness of variable …

[引用][C] Genomic screening for'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)

CG Bonnemann, MR Passos-Bueno… - Human Molecular …, 1996 - repositorio.usp.br
ReP USP - Detalhe do registro: Genomic screening for 'BETA'-sarcoglycan gene mutations:
missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e) Home …

[引用][C] Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG BÖNNEMANN… - Human molecular …, 1996 - pascal-francis.inist.fr
Genomic screening for β-sarcoglycan gene mutations : missense mutations may cause severe
limb-girdle muscular dystrophy type 2E (LGMD 2E) CNRS Inist Pascal-Francis CNRS Pascal and …
[PDF] psu.edu

[PDF][PDF] Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bönnemann, MR Passos-Bueno… - Human Molecular …, 1996 - Citeseer
Limb-girdle muscular dystrophies (LGMDs) are a genetically heterogeneous group of
disorders, characterized clinically by predominantly proximal muscle weakness of variable …

Genomic screening for β-sarcoglycan gene mutations: Missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bönnemann, MR Passos-Bueno… - Human molecular …, 1996 - scholars.northwestern.edu
Autosomal recessive limb-girdle muscular dystrophies (LGMDs) are genetically
heterogeneous. A subgroup of these disorders is caused by mutations in the dystrophin …
[PDF] academia.edu

[PDF][PDF] Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

CG Bönnemann, MR Passos-Bueno… - Human Molecular …, 1996 - academia.edu
Limb-girdle muscular dystrophies (LGMDs) are a genetically heterogeneous group of
disorders, characterized clinically by predominantly proximal muscle weakness of variable …

[引用][C] Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

C Bonnemann - Human Molecular Genetics, 1996 - cir.nii.ac.jp
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause
severe limb-girdle muscular dystrophy type 2E (LGMD 2E) | CiNii Research CiNii 国立情報学 …

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).

CG Bönnemann, MR Passos-Bueno… - Human Molecular …, 1996 - europepmc.org
Autosomal recessive limb-girdle muscular dystrophies (LGMDs) are genetically
heterogeneous. A subgroup of these disorders is caused by mutations in the dystrophin …