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dc.contributor.authorBUYSSE, K
dc.contributor.authorGILISSEN, C
dc.contributor.authorMANCINI, GM
dc.contributor.authorDELRÉE, P
dc.contributor.authorWILLEMSEN, MA
dc.contributor.authorRAMADZA, DP
dc.contributor.authorCHITAYAT, D
dc.contributor.authorBENNETT, C
dc.contributor.authorSHERIDAN, E
dc.contributor.authorLIN, YY
dc.contributor.authorPEETERS, EA
dc.contributor.authorTAN-SINDHUNATA, GM
dc.contributor.authorde, Die-Smulders
dc.contributor.authorDEVRIENDT, K
dc.contributor.authorKAYSERILI, H
dc.contributor.authorEL-HASHASH, OA
dc.contributor.authorSTEMPLE, DL
dc.contributor.authorLEFEBER, DJ
dc.contributor.authorvan, Bokhoven
dc.contributor.authorAltunoglu, UMUT
dc.contributor.authorvan, den
dc.contributor.authorvan, Beusekom
dc.contributor.authorRIEMERSMA, M
dc.contributor.authorPFUNDT, R
dc.contributor.authorVISSERS, LE
dc.contributor.authorROSCIOLI, T
dc.contributor.authorKAMSTEEG, EJ
dc.contributor.authorMAYSTADT, I
dc.contributor.authorvan, Reeuwijk
dc.contributor.authorSCHRADERS, M
dc.contributor.authorBUCKLEY, MF
dc.contributor.authorBRUNNER, HG
dc.contributor.authorGRISART, B
dc.contributor.authorZHOU, H
dc.contributor.authorVELTMAN, JA
dc.date.accessioned2021-03-05T20:45:39Z
dc.date.available2021-03-05T20:45:39Z
dc.identifier.citationROSCIOLI T., KAMSTEEG E., BUYSSE K., MAYSTADT I., van R., van d., van B., RIEMERSMA M., PFUNDT R., VISSERS L., et al., "Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan.", Nature genetics, cilt.44, ss.581-5, 2012
dc.identifier.issn1061-4036
dc.identifier.otherav_d5b8e126-ea4b-4044-a6c1-78c650b106bb
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/141029
dc.identifier.urihttps://doi.org/10.1038/ng.2253
dc.language.isoeng
dc.titleMutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan.
dc.typeMakale
dc.relation.journalNature genetics
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.startpage581
dc.identifier.endpage5
dc.contributor.firstauthorID181704


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