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Article

[Sarcoglycanopathies].

Revista de neurologia - 1 Jan 2000

Colomer J

Abstract excerpt

INTRODUCTION: Identification of several clinical pictures in relation to a deficit of various protein components of the sarcoglycan complex, has allowed a new classification to be established for muscular dystrophies, correlating the protein alpha, beta, gamma, sigma deficit with a type of girdle...

Topics

Adult
Child
Child, Preschool
Dystrophin
Glycoproteins
Humans
Muscular Dystrophies
Phenotype
Point Mutation
Sarcolemma

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10101783

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026. Prepared record publication-10101783-2026-08-31.1. Manifest publication-graph-cohort-2026-08-31.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 31 Aug 2026.

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Related research

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Research trail→

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[Sarcoglycanopathies].PMID 10101783Read ↗

[Sarcoglycanopathies: state of the art and therapeutic perspectives].Semantic proximity Read ↗

[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation].Semantic proximity Read ↗

[Sarcoglycanopathies, a particular limb-girdle muscular dystrophy type (phenotype in three Polish families): initial report].Semantic proximity Read ↗

Sarcoglycanopathies: molecular pathogenesis and therapeutic prospectsSemantic proximity Read ↗

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.Semantic proximity Read ↗

Invited commentary. Sarcoglycanopathies: a clinico-pathological study.Semantic proximity Read ↗

Phenotypic and immunohistochemical characterization of sarcoglycanopathies.Semantic proximity Read ↗

[Muscular dystrophies].Semantic proximity Read ↗

Sarcoglycanopathies: an update.Semantic proximity Read ↗

[Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases].Semantic proximity Read ↗

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationSemantic proximity Read ↗

Sarcoglycanopathies: a clinico-pathological study.Semantic proximity Read ↗

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