Retinitis Pigmentosa 28

Common Name(s)

Retinitis Pigmentosa 28

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Retinitis Pigmentosa 28" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Retinitis Pigmentosa 28" returned 1 free, full-text research articles on human participants. First 3 results:

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

Author(s): Frank Zach, Felix Grassmann, Thomas Langmann, Nasrin Sorusch, Uwe Wolfrum, Heidi Stöhr

Journal: Hum. Mol. Genet.. 2012 Nov;21(21):4573-86.

 

Loss-of-function mutations in the gene encoding FAM161A were recently discovered as the cause for RP28, an autosomal recessive form of retinitis pigmentosa. To initiate the characterization of the cellular role of FAM161A in the retina, we focused on its subcellular localization and ...

Last Updated: 16 Oct 2012

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Retinitis Pigmentosa 28" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.