Bladder tumour-derived somatic TSC1 missense mutations cause loss of function via distinct mechanisms-Reference-Cited by-同舟云学术

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Bladder tumour-derived somatic TSC1 missense mutations cause loss of function via distinct mechanisms

Published:2008-04-07 Issue:13 Volume:17 Page:2006-2017
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Pymar Louis S.,Platt Fiona M.,Askham Jon M.,Morrison Ewan E.,Knowles Margaret A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/13/2006/17244857/ddn098.pdf

Reference76 articles.

1. Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34;van Slegtenhorst;Science,1997

2. Identification and characterization of the tuberous sclerosis gene on chromosome 16. The European Chromosome 16 Tuberous Sclerosis Consortium;Consortium.;Cell,1993

3. Molecular genetic advances in tuberous sclerosis;Cheadle;Hum. Genet.,2000

4. Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosis;Jones;Hum. Mol. Genet.,1997

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