【J Neurol Sci】creening of hereditary spastic 等3篇谢谢yufei5322032，zunwang
篇号： 1作者： Beetz C, Schule R, Klebe S, Klimpe S, Klopstock T, Lacour A, Otto S, Sperfeld AD, van de Warrenburg B, Schols L,Deufel T
文题： Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots
杂志全名（或缩写）： J Neurol Sci
年份，卷（期）：起止页码： 2008 May 15;268(1-2):131-5.
全文链接： [url]http://www.ncbi.nlm.nih.gov//entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=18191948[/url]；[url]http://openurl.ebscohost.com/linksvc/linking.aspx?genre=article&sid=PubMed&issn=0022-510X&title=J%20Neurol%20Sci&volume=268&issue=1-2&spage=131&atitle=Screening%20of%20hereditary%20spastic%20paraplegia%20patients%20for%20alterations%20at%20NIPA1%20mutational%20hotspots.&aulast=Beetz&date=2008[/url]；[url]http://linkinghub.elsevier.com/retrieve/pii/S0022-510X[/url](07)00772-1；[url]http://www.swetswise.com/link/access_db?issn=0022-510X&vol=268&iss=1&page=131&FT=1[/url]
PMID： 18191948
篇号： 2
作者： Klebe S, Lacour A, Durr A, Stojkovic T, Depienne C, Forlani S, Poea-Guyon S, Vuillaume I, Sablonniere B, Vermersch P, Brice A,Stevanin G
文题： NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe
杂志全名（或缩写）： Neurogenetics
年份，卷（期）：起止页码： 2007 Apr;8(2):155-7.
全文链接： [url]http://www.ncbi.nlm.nih.gov//entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17205300[/url]；[url]http://openurl.ebscohost.com/linksvc/linking.aspx?genre=article&sid=PubMed&issn=1364-6745&title=Neurogenetics&volume=8&issue=2&spage=155&atitle=NIPA1%20[/url](SPG6)%20mutations%20are%20a%20rare%20cause%20of%20autosomal%20dominant%20spastic%20paraplegia%20in%20Europe.&aulast=Klebe&date=2007；[url]http://openurl.ingenta.com/content/nlm?genre=article&issn=1364-6745&volume=8&issue=2&spage=155&aulast=Klebe[/url]；[url]http://openurl.proquest.com/in?service=pq&issn=1364-6745&volume=8&issue=2&spage=155[/url]；[url]http://dx.doi.org/10.1007/s10048-006-0074-9[/url]；[url]http://www.swetswise.com/link/access_db?issn=1364-6745&vol=8&iss=2&page=155&FT=1[/url]
PMID： 17205300
篇号： 3
作者： Goytain A, Hines RM, El-Husseini A,Quamme GA
文题： NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
杂志全名（或缩写）： J Biol Chem
年份，卷（期）：起止页码： 2007 Mar 16;282(11):8060-8.
全文链接： [url]http://www.ncbi.nlm.nih.gov//entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17166836[/url]；[url]http://www.jbc.org/cgi/pmidlookup?view=long&pmid=17166836[/url]；[url]http://openurl.ebscohost.com/linksvc/linking.aspx?genre=article&sid=PubMed&issn=0021-9258&title=J%20Biol%20Chem&volume=282&issue=11&spage=8060&atitle=NIPA1[/url](SPG6),%20the%20basis%20for%20autosomal%20dominant%20form%20of%20hereditary%20spastic%20paraplegia,%20encodes%20a%20functional%20Mg2+%20transporter.&aulast=Goytain&date=2007
PMID： 17166836
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