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Molecular genetics of neurofibromatosis type 1 (NF1).

Neurofibromatosis type 1 (NF1), also called von Recklinghausen disease or peripheral neurofibromatosis, is a common autosomal dominant disorder characterised by multiple neurofibromas, café au lait spots, and Lisch nodules of the iris, with a variable clinical expression. The gene responsible for th...

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Autori principali: Shen, M H, Harper, P S, Upadhyaya, M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1996
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051805/
https://ncbi.nlm.nih.gov/pubmed/8825042
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