Literature DB >> 11255506

Retinitis pigmentosa: mutations in a receptor tyrosine kinase gene, MERTK.

A Kumar1.   

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Year:  2001        PMID： 11255506     DOI： 10.1007/bf02708973

Source DB:  PubMed          Journal:  J Biosci        ISSN： 0250-5991            Impact factor:   1.826


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  5 in total

1.  Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.

Authors:  T P Dryja; L B Hahn; K Kajiwara; E L Berson
Journal:  Invest Ophthalmol Vis Sci       Date:  1997-09       Impact factor: 4.799

Review 2.  Molecular genetics of retinitis pigmentosa.

Authors:  T P Dryja; T Li
Journal:  Hum Mol Genet       Date:  1995       Impact factor: 6.150

3.  Assignment of protooncogene MERTK (a.k.a. c-mer) to human chromosome 2q14.1 by in situ hybridization.

Authors:  H U Weier; J Fung; R A Lersch
Journal:  Cytogenet Cell Genet       Date:  1999

4.  Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.

Authors:  A Gal; Y Li; D A Thompson; J Weir; U Orth; S G Jacobson; E Apfelstedt-Sylla; D Vollrath
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

5.  Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.

Authors:  P M D'Cruz; D Yasumura; J Weir; M T Matthes; H Abderrahim; M M LaVail; D Vollrath
Journal:  Hum Mol Genet       Date:  2000-03-01       Impact factor: 6.150
  5 in total

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