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Four-year follow-up study in a NF1 Boy with a focal pontine hamartoma
Neurofibromatosis is a collective name for a group of genetic conditions in which benign tumours affect the nervous system. Type 1 is caused by a genetic mutation in the NF1 gene (OMIM 613113) and symptoms can vary dramatically between individuals, even within the same family. Some people have very...
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| Main Authors: | , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BioMed Central
2013
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3579694/ https://ncbi.nlm.nih.gov/pubmed/23399325 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-39-10 |
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