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Development and validation in 500 female samples of a TP-PCR assay to identify AFF2 GCC expansions
Over 100 X-linked intellectual disability genes have been identified, with triplet repeat expansions at the FMR1 (FRAXA) and AFF2 (FRAXE) genes being the causative agent in two of them. The absence of FRAXE pathognomonic features hampers early recognition, delaying testing and molecular confirmation...
Tallennettuna:
| Julkaisussa: | Sci Rep |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Nature Publishing Group UK
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8289994/ https://ncbi.nlm.nih.gov/pubmed/34282157 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-93473-5 |
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