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Article

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3

1 Apr 1990

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

Identifiers

PMID: 2320125
DOI: 10.1038/344540a0

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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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Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3PMID 2320125Read ↗

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A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21.Semantic proximity Read ↗

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Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23–q24Semantic proximity Read ↗

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3Semantic proximity Read ↗

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