Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.

Eisenbarth, I; Beyer, K; Krone, W; Assum, G

Eisenbarth, I; Beyer, K; Krone, W; Assum, G.

Affiliation

Eisenbarth I; Abteilung Humangenetik, Universität Ulm, Albert-Einstein-Allee 11, D-89081 Ulm, Germany. ingrid.eisenbarth@medizin.uni-ulm.de

Am J Hum Genet ; 66(2): 393-401, 2000 Feb.

Article in En | MEDLINE | ID: mdl-10677298

Subject(s)

Mutation/genetics; Neurofibromatosis 1/genetics; Neurofibromatosis 1/pathology; Proteins/genetics; Adult; Alleles; Codon, Terminator/genetics; Female; Gene Frequency; Genetic Variation/genetics; Humans; Loss of Heterozygosity/genetics; Male; Middle Aged; Molecular Sequence Data; Neurofibromatosis 1/metabolism; Neurofibromin 1; Peptide Fragments/analysis; Peptide Fragments/chemistry; Peptide Fragments/genetics; Phenotype; Point Mutation/genetics; Polymorphism, Genetic/genetics; Proteins/analysis; Proteins/chemistry; Sequence Deletion/genetics; Tumor Cells, Cultured

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Neurofibromatosis 1 / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2000 Document type: Article

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