ArticleThe Japanese journal of human genetics1997
Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3.
Article in The Japanese journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
- Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.The Japanese journal of human genetics · 1997Article
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3 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
Connexin43 is one of connexin proteins which make up the intercellular gap junctions. Targeted null mutation of the mouse connexin43 gene has been reported to result in a cardiac malformation. Moreover, single-base mutations of the human homolog (GJA1) were identified in patients with laterality defects of the chest and abdominal organs, suggesting that connexin43 contributes to the determination of laterality during organogenesis. We mapped GJA1 to 6q22.3 by fluorescence in situ hybridization, using a bacterial artificial chromosome (BAC) clone that covered almost the entire GJA1-cDNA, as a probe.
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