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Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension
A heritable connective-tissue-disorder often is suspected in patients with spontaneous spinal CSF leaks and intracranial hypotension, but the nature of the disorder remains unknown in most patients. The aim of this study was to assess the gene encoding TGF-β receptor-2 (TGFBR2) as a candidate gene f...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Milan
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3476180/ https://ncbi.nlm.nih.gov/pubmed/18264665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10194-008-0017-y |
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