Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations

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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorMELO, U. S.
dc.contributor.authorFREUA, F.
dc.contributor.authorLYNCH, D. S.
dc.contributor.authorRIPA, B. D.
dc.contributor.authorTENORIO, R. B.
dc.contributor.authorSAUTE, J. A. M.
dc.contributor.authorLEITE, F. de Souza
dc.contributor.authorKITAJIMA, J.
dc.contributor.authorHOULDEN, H.
dc.contributor.authorZATZ, M.
dc.contributor.authorKOK, F.
dc.date.accessioned2018-11-21T17:04:43Z
dc.date.available2018-11-21T17:04:43Z
dc.date.issued2018
dc.description.indexMEDLINE
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Sao Paulo/Centro de Pesquisa, Inovacao e Difusao
dc.description.sponsorshipNational Council of Technological and Scientific Development
dc.identifier.citationCLINICAL GENETICS, v.94, n.5, p.482-483, 2018
dc.identifier.doi10.1111/cge.13428
dc.identifier.eissn1399-0004
dc.identifier.issn0009-9163
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29487
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofClinical Genetics
dc.rightsrestrictedAccess
dc.rights.holderCopyright WILEY
dc.subjectggg
dc.subject.otherataxia
dc.subject.wosGenetics & Heredity
dc.titleClinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations
dc.typearticle
dc.type.categoryletter
dc.type.versionpublishedVersion
dspace.entity.typePublication
hcfmusp.affiliation.countryInglaterra
hcfmusp.affiliation.countryisogb
hcfmusp.author.externalMELO, U. S.:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil
hcfmusp.author.externalLYNCH, D. S.:UCL Inst Neurol, Dept Mol Neurosci, London, England
hcfmusp.author.externalTENORIO, R. B.:Hosp Clin Porto Alegre, Serv Genet Med & Neurol, Porto Alegre, RS, Brazil
hcfmusp.author.externalSAUTE, J. A. M.:Hosp Clin Porto Alegre, Serv Genet Med & Neurol, Porto Alegre, RS, Brazil
hcfmusp.author.externalLEITE, F. de Souza:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil
hcfmusp.author.externalKITAJIMA, J.:Mendelics, Sao Paulo, Brazil
hcfmusp.author.externalHOULDEN, H.:UCL Inst Neurol, Dept Mol Neurosci, London, England
hcfmusp.author.externalZATZ, M.:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil
hcfmusp.citation.scopus9
hcfmusp.contributor.author-fmusphcFERNANDO FREUA
hcfmusp.contributor.author-fmusphcBRUNO DELLA RIPA RODRIGUES ASSIS
hcfmusp.contributor.author-fmusphcFERNANDO KOK
hcfmusp.description.beginpage482
hcfmusp.description.endpage483
hcfmusp.description.issue5
hcfmusp.description.volume94
hcfmusp.origemWOS
hcfmusp.origem.pubmed30198554
hcfmusp.origem.scopus2-s2.0-85053060511
hcfmusp.origem.wosWOS:000446554800013
hcfmusp.publisher.cityHOBOKEN
hcfmusp.publisher.countryUSA
hcfmusp.relation.referenceGan-Or Z, 2016, AM J HUM GENET, V98, P1038, DOI 10.1016/j.ajhg.2016.04.002
hcfmusp.relation.referenceKocoglu C, 2018, NEUROL-GENET, V4, DOI 10.1212/NXG.0000000000000218
hcfmusp.relation.referenceShetty A, 2018, NEUROLOGY S15, V90
hcfmusp.relation.referenceTadic V, 2017, J NEUROL, V264, P1008, DOI 10.1007/s00415-017-8464-5
hcfmusp.relation.referenceTravaglini L, 2017, J NEUROL SCI, V378, P210, DOI 10.1016/j.jns.2017.05.014
hcfmusp.relation.referenceWang YB, 2016, CELL REP, V16, P79, DOI 10.1016/j.celrep.2016.05.044
hcfmusp.scopus.lastupdate2024-05-10
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