Schindler Disease

Common Name(s)

Schindler Disease

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Schindler Disease" for support, advocacy or research.

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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 "Schindler Disease" returned 2 free, full-text research articles on human participants. First 3 results:

Mutations in PLA2G6 and the riddle of Schindler disease.
 

Author(s): S K Westaway, A Gregory, S J Hayflick

Journal: J. Med. Genet.. 2007 Jan;44(1):e64.

 

Last Updated: 8 Jan 2007

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Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy.
 

Author(s): A M Wang, D Schindler, R Desnick

Journal: J. Clin. Invest.. 1990 Nov;86(5):1752-6.

 

Schindler disease is a recently recognized infantile neuroaxonal dystrophy resulting from the deficient activity of the lysosomal hydrolase, alpha-N-acetylgalctosaminidase (alpha-GalNAc). The recent isolation and expression of the full-length cDNA encoding alpha-GalNAc facilitated ...

Last Updated: 28 Dec 1990

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Reviews from the PubMed Database

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The terms "Schindler Disease" 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.