Deletions of NF1 gene and exons detected by multiplex ligation‐dependent probe amplification

To estimate the contribution of single and multi‐exon NF1 gene copy‐number changes to the NF1 mutation spectrum, we analysed a series of 201 Italian patients with neurofibromatosis type 1 (NF1). Of these, 138 had previously been found, using denaturing high‐performance liquid chromatography or prote...

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Detalles Bibliográficos
Main Authors: De Luca, A, Bottillo, I, Dasdia, M C, Morella, A, Lanari, V, Bernardini, L, Divona, L, Giustini, S, Sinibaldi, L, Novelli, A, Torrente, I, Schirinzi, A, Dallapiccola, B
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 2007
Assuntos:
Mutation Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652822/
https://ncbi.nlm.nih.gov/pubmed/18055911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.053785
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