Literature DB >> 17249559

Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations.

Aileen Aherne1, Avril Kennan, Paul F Kenna, Niamh McNally, G Jane Farrar, Pete Humphries.   

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Year:  2006        PMID： 17249559     DOI： 10.1007/0-387-32442-9_13

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


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  2 in total

1.  Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1).

Authors:  Lea D Bennett; Martin Klein; Finny T John; Bojana Radojevic; Kaylie Jones; David G Birch
Journal:  Transl Vis Sci Technol       Date:  2020-04-23       Impact factor: 3.283

Review 2.  The Role of the U5 snRNP in Genetic Disorders and Cancer.

Authors:  Katherine A Wood; Megan A Eadsforth; William G Newman; Raymond T O'Keefe
Journal:  Front Genet       Date:  2021-01-28       Impact factor: 4.599
  2 in total

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