2eea

Revision as of 22:42, 12 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="2eea" size="450" color="white" frame="true" align="right" spinBox="true" caption="2eea" /> '''Solution structure of the 17th filamin doma...)
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Solution structure of the 17th filamin domain from human Filamin-B

File:2eea.gif


2eea

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DiseaseDisease

Known diseases associated with this structure: Atelosteogenesis, type III OMIM:[603381], Atelostogenesis, type I OMIM:[603381], Bare lymphocyte syndrome, type I OMIM:[170260], Boomerang dysplasia OMIM:[603381], Larson syndrome OMIM:[603381], Spondylocarpotarsal synostosis syndrome OMIM:[603381]

About this StructureAbout this Structure

2EEA is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

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