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Genomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease

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dc.contributor.authorENDER, KARACA
dc.contributor.authorPEHLİVAN, DAVUT
dc.contributor.authorTA, HAREL
dc.contributor.authorSM, WEITZER
dc.contributor.authorHM, SHIRAISHI
dc.contributor.authorGAMBIN, THOMAS
dc.contributor.authorBAYRAM, YAVUZ
dc.contributor.authorWISZNIEWSKI, WA
dc.contributor.authorNU, JHANGIANI
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.institutionauthorYEŞİL, GÖZDE
dc.date.accessioned2019-10-05T21:37:20Z
dc.date.available2019-10-05T21:37:20Z
dc.date.issued2014-10-22
dc.identifier.citationENDER K., PEHLİVAN D., TA H., SM W., HM S., GAMBIN T., BAYRAM Y., WISZNIEWSKI W., NU J., YEŞİL G., -Genomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease-, american society of human genetics, 18 - 22 October 2014
dc.identifier.urihttps://hdl.handle.net/20.500.12645/7781
dc.language.isoen
dc.titleGenomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease
dc.typeConference Paper
dspace.entity.typePublication
local.avesis.idc17e9763-4350-4bdb-9070-b1ce2ea11902
local.avesis.response7657
relation.isAuthorOfPublicationb653abbc-327a-4b3b-a227-f3344d8d6b70
relation.isAuthorOfPublication.latestForDiscoveryb653abbc-327a-4b3b-a227-f3344d8d6b70
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