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Mutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia.

dc.contributor.authorAlvarado, D
dc.contributor.authorLemons, R
dc.contributor.authorHedera, P
dc.contributor.authorWeber, C
dc.contributor.authorTukel, T
dc.contributor.authorApak, M
dc.contributor.authorHeiman-Patterson, T
dc.contributor.authorMing, L
dc.contributor.authorBuil, M
dc.contributor.authorFink, JK
dc.contributor.authorZhao, X
dc.contributor.authorRainier, S
dc.date.accessioned2021-03-04T18:40:43Z
dc.date.available2021-03-04T18:40:43Z
dc.date.issued2001
dc.identifier.citationZhao X., Alvarado D., Rainier S., Lemons R., Hedera P., Weber C., Tukel T., Apak M., Heiman-Patterson T., Ming L., et al., "Mutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia.", AMERICAN JOURNAL OF HUMAN GENETICS, cilt.69, ss.195, 2001
dc.identifier.issn0002-9297
dc.identifier.otherav_8bf5781a-90b0-4b05-b783-18555ad5bb46
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/94706
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleMutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia.
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF HUMAN GENETICS
dc.contributor.department, ,
dc.identifier.volume69
dc.identifier.issue4
dc.identifier.startpage195
dc.identifier.endpage195
dc.contributor.firstauthorID163281


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