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Article

Fine-structure mapping of the hereditary inclusion body myopathy locus.

Genomics - 1 Jan 1999

Eisenberg I, Thiel C, Levi T, Tiram E, Argov Z, Sadeh M, Jackson C L, Thierfelder L, Mitrani-Rosenbaum S

Abstract excerpt

The gene responsible for a recessive form of hereditary inclusion body myopathy (HIBM) has previously been mapped to a 10-cM interval on chromosome 9p1-q1. We report the results of further mapping studies using two-point linkage analyses and linkage disequilibrium analyses with 20 HIBM families. We demonstrate that the HIBM gene (HGMW-approved symbol IBM2) lies between loci D9S1791 and D9S50, which are about 1 Mb...

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Identifiers

PMID: 9888997
DOI: 10.1006/geno.1998.5630

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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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