The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or tth20 deletions
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference12 articles.
1. A cluster of related zinc finger protein genes is deleted in the mouse early acting embryonic lethal mutation w18;Crossley;Proc. Natl. Acad. Sci. USA,1991
2. Identification and characterisation of the tuberous sclerosis gene on chromosome 16;Cell,1993
3. An alpha globin pseudogene is located within the mouse t complex;Fox;Immunogenetics,1984
4. Evidence that the gene for tuberous sclerosis is on chromosome 9;Fryer;Lancet,1987
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1. Chromosomal localization of three vacuolar-H+-ATPase 16 kDa subunit (ATP6V0C) genes in the murine genome;Cytogenetic and Genome Research;2002
2. Mouse Sox8 is located between, not within,the t-complex deletions tw18 and th20 on chromosome 17;Cytogenetic and Genome Research;2001
3. Genetic variants of the tuberous sclerosis 2 tumour suppressor gene in mouse t haplotypes;Genetical Research;1999-10
4. Cloning and characterization of a mouse homologue (mnthl1) of Escherichia coli endonuclease III 1 1Edited by J. Miller;Journal of Molecular Biology;1998-10
5. A genetic, physical, and comparative map of rat chromosome 10;Mammalian Genome;1996-06
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