Amplifying the spectrum of SPAST gene mutations.

导出 OA

翻译打印收藏纠错

第一作者： Lorenzo,Verriello

第一单位： Neurology Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. lorenzo.verriello@asufc.sanita.fvg.it.

作者： Lorenzo,Verriello ^[1] ; Incoronata Renata,Lonigro ^[2] ; Maria Elena,Pessa ^[3] ; Elena,Betto ^[4] ; Giada,Pauletto ^[5] ; Federico,Fogolari ^[6] ; Gian Luigi,Gigli ^[7] ; Francesco,Curcio ^[8]

作者单位： Neurology Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. lorenzo.verriello@asufc.sanita.fvg.it. ^[1] Institute of Clinical Pathology, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. incoronata.lonigro@asufc.sanita.fvg.it. ^[2] a:1:{s:5:"en_US";s:49:"Azienda ospedaliero universitaria Friuli centrale";}. marialen@gmail.com. ^[3] Institute of Clinical Pathology, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. elena.betto@asufc.sanita.fvg.it. ^[4] Neurology Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. giada.pauletto@asufc.sanita.fvg.it. ^[5] Department of Mathematics, Informatics and Physics (DMIF), University of Udine, Italy. federico.fogolari@uniud.it. ^[6] Clinical Neurology Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. gianluigi.gigli@asufc.sanita.fvg.it. ^[7] Institute of Clinical Pathology, Santa Maria della Misericordia University Hospital, ASUFC, Udine, Italy. francesco.curcio@asufc.sanita.fvg.it. ^[8]

主题词腺苷三磷酸酶类(Adenosine Triphosphatases);人类(Humans);突变(Mutation);截瘫(Paraplegia);痉挛性截瘫, 遗传性(Spastic Paraplegia, Hereditary)

DOI 10.23750/abm.v92iS1.11608

PMID 35132972

发布时间 2023-09-29

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交