Dataset Information

Next Generation Mendelian Genetics: Atypical Werner Syndrome

ABSTRACT:

Werner syndrome (WS) is an adult-onset progeroid syndrome characterized by accelerated aging. The International Registry of Werner Syndrome in the Department of Pathology, University of Washington, collects WS cases from all over the world. Classical WS is caused by WRN mutations. Those who do not carry WRN are categorized as "atypical Werner syndrome." A small subset of atypical WS is caused by LMNA mutations. There also are many cases whose causes are still unknown. The purpose of this study is to identify other causative gene(s) of atypical WS.

PROVIDER: phs000434 | dbGaP |

SECONDARY ACCESSION(S): PRJNA80283PRJNA80285

REPOSITORIES: dbGaP

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Source:

			Action	DRS
	GapExchange_phs000434.v1.p1.xml	Xml
	dbGaPEx2.1.5.xsd	Other
	Study_Report.phs000434.Mendelian_AtypicalWernerSynd.v1.p1.MULTI.pdf	Pdf
	manifest_phs000434.Mendelian_AtypicalWernerSynd.v1.p1.c1.AAS.pdf	Pdf
	datadict_v2.xsl	Other

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Next Generation Mendelian Genetics: Atypical Werner Syndrome

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