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ATP-dependent helicase activity is dispensable for the physiological functions of Recql4
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder characterized by skin rash (poikiloderma), skeletal dysplasia, small stature, juvenile cataracts, sparse or absent hair, and predisposition to specific malignancies such as osteosarcoma and hematological neoplasms. RTS is caused...
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| Publicado no: | PLoS Genet |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6636780/ https://ncbi.nlm.nih.gov/pubmed/31276497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1008266 |
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