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Genotype–phenotype correlations in Peutz-Jeghers syndrome
Background and aims: Peutz-Jeghers syndrome (PJS) is a dominantly inherited disorder often caused by mutations in STK11. Time to onset of symptoms was characterised for a large collection of individuals with PJS who had been tested for STK11 mutations and genotype–phenotype correlations were evaluat...
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| Päätekijät: | , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
2004
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735760/ https://ncbi.nlm.nih.gov/pubmed/15121768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.010900 |
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