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1x5n

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1x5n

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Solution structure of the second PDZ domain of harmonin protein

Disease

Known diseases associated with this structure: Deafness, autosomal recessive 18 OMIM:[605242], Usher syndrome, type 1C OMIM:[605242]

About this Structure

1X5N is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Nov 12 20:00:07 2007

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