The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association

Author:

Zach Frank,Grassmann Felix,Langmann Thomas,Sorusch Nasrin,Wolfrum Uwe,Stöhr Heidi

Publisher

Oxford University Press (OUP)

Subject

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

Reference47 articles.

1. Retinitis pigmentosa and allied conditions today: a paradigm of translational research;Ayuso;Genome Med.,2010

2. Intraflagellar transport and the sensory outer segment of vertebrate photoreceptors;Insinna;Dev. Dyn.,2008

3. The retinal ciliopathies;Adams;Ophthalmic Genet.,2007

4. Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa;Langmann;Am. J. Hum. Genet.,2010

5. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family;Gu;J. Med. Genet.,1999

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