Literature DB >> 7711726

High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons.

J Sainz1, K Figueroa, M E Baser, V F Mautner, S M Pulst.   

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Year:  1995        PMID： 7711726     DOI： 10.1093/hmg/4.1.137

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  6 in total

1.  Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas.

Authors:  L R De Vitis; A Tedde; F Vitelli; F Ammannati; P Mennonna; U Bigozzi; E Montali; L Papi
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

Review 2.  Neurofibromatosis type 2.

Authors:  D G Evans; M Sainio; M E Baser
Journal:  J Med Genet       Date:  2000-12       Impact factor: 6.318

3.  Universal absence of merlin, but not other ERM family members, in schwannomas.

Authors:  A O Stemmer-Rachamimov; L Xu; C Gonzalez-Agosti; J A Burwick; D Pinney; R Beauchamp; L B Jacoby; J F Gusella; V Ramesh; D N Louis
Journal:  Am J Pathol       Date:  1997-12       Impact factor: 4.307

4.  Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.

Authors:  D M Parry; M M MacCollin; M I Kaiser-Kupfer; K Pulaski; H S Nicholson; M Bolesta; R Eldridge; J F Gusella
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

5.  Recessive oncogenes: current status.

Authors:  Xiang Gao; Kenneth V Honn
Journal:  Pathol Oncol Res       Date:  1995       Impact factor: 3.201

6.  Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.

Authors:  D G Evans; L Trueman; A Wallace; S Collins; T Strachan
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318
  6 in total

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