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Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13.
CAGR1 is a recently characterised polymorphic trinucleotide repeat localised to 13q13, which has been suggested as a possible candidate gene for neurological disorders that manifest genetic anticipation. To provide evidence in support of this hypothesis, a large number of chromosomes (n = 928) from...
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| Huvudupphovsman: | |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
1997
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1050949/ https://ncbi.nlm.nih.gov/pubmed/9152839 |
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