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Autor:
Kobus, K., Hartl, D., Ott, C.E., Osswald, M., Huebner, A., Hagen, M. von der, Emmerich, D., Kuhnisch, J., Morreau, H., Hes, F.J., Mautner, V.F., Harder, A., Tinschert, S., Mundlos, S., Kolanczyk, M.
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 3, p e0119030 (2015)
PLoS One
PLoS ONE, 10(3)
PLoS ONE, Vol 10, Iss 3, p e0119030 (2015)
PLoS One
PLoS ONE, 10(3)
BackgroundNeurofibromatosis type I (NF1, MIM#162200) is a relatively frequent genetic condition, which predisposes to tumor formation. Apart from tumors, individuals with NF1 often exhibit endocrine abnormalities such as precocious puberty (2,5-5% of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::77dfdb0b7c8e5c4f35061f94659cf0bf
https://pubmed.ncbi.nlm.nih.gov/25775093
https://pubmed.ncbi.nlm.nih.gov/25775093
