Lethal congenital contractural syndrome 3

Common Name(s)

Lethal congenital contractural syndrome 3

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Lethal congenital contractural syndrome 3" 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 "Lethal congenital contractural syndrome 3" returned 1 free, full-text research articles on human participants. First 3 results:

Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway.
 

Author(s): Ginat Narkis, Rivka Ofir, Esther Manor, Daniella Landau, Khalil Elbedour, Ohad S Birk

Journal: Am. J. Hum. Genet.. 2007 Sep;81(3):589-95.

 

Lethal congenital contractural syndrome type 2 (LCCS2) is an autosomal recessive neurogenic form of arthrogryposis that is associated with atrophy of the anterior horn of the spinal cord. We previously mapped LCCS2 to 6.4 Mb on chromosome 12q13 and have now narrowed the locus to 4.6 ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

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The terms "Lethal congenital contractural syndrome 3" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

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