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Article

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone

1 Jul 2000

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 11252708
DOI: 10.1097/00125817-200007000-00006

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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.

Related research

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Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bonePMID 11252708Read ↗

Genetic Determinants of Paget's Disease of Bone.Semantic proximity Read ↗

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Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.Semantic proximity Read ↗

The genetics of Paget's disease of the bone.Semantic proximity Read ↗

Familial Early-Onset Paget's Disease of Bone Associated with a Novel hnRNPA2B1 Mutation.Semantic proximity Read ↗

The limb-girdle muscular dystrophies: diagnostic guidelines.Semantic proximity Read ↗

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal DementiaSemantic proximity Read ↗

Rare Inherited forms of Paget’s Disease and Related SyndromesSemantic proximity Read ↗

Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget's Disease of Bone.Semantic proximity Read ↗

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35Semantic proximity Read ↗

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