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Article

IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.

American journal of human genetics - 1 May 2009

Brkanac Zoran, Spencer David, Shendure Jay, Robertson Peggy D, Matsushita Mark, Vu Tiffany, Bird Thomas D, Olson Maynard V, Raskind Wendy H

Abstract excerpt

We have established strong linkage evidence that supports mapping autosomal-dominant sensory/motor neuropathy with ataxia (SMNA) to chromosome 7q22-q32. SMNA is a rare neurological disorder whose phenotype encompasses both the central and the peripheral nervous system. In order to identify a gene responsible for SMNA, we have undertaken a comprehensive genomic evaluation of the region of linkage, including...

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Identifiers

PMID: 19409521
DOI: 10.1016/j.ajhg.2009.04.008
PMCID: PMC2680994

Genes

IFRD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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