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Article

Prognostic factors in mild dystrophinopathies.

Journal of the neurological sciences - 1 Oct 1996

Angelini C, Fanin M, Freda M P, Martinello F, Miorin M, Melacini P, Siciliano G, Pegoraro E, Rosa M, Danieli G A

Abstract excerpt

One hundred twenty five patients from 105 families were considered, showing in-frame intragenic deletion or duplication of the dystrophin gene and/or abnormal dystrophin on muscle biopsy. According to clinical status of patients, the affection was classified as subclinical, benign, moderate or severe. Significant decrease of dystrophin abundance was observed with increasing clinical severity (p < 0.05). Detailed...

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Identifiers

PMID: 8902723
DOI: 10.1016/0022-510x(96)00144-x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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