Neurogenetics,volume 5,issue 3  (09-2004)

Period of time： 2004年3期

Publisher： Springer Publishing Company

Founded in： 1997

Total resources： 16

ISSN： 1364-6745

Subject： R74 Neurology and Psychiatry

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Neurogenetics,volume 5,issue 3

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Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype

By Oliveira Sofia,Scott William,Zhang Fengyu,Stajich Jeffrey,Fujiwara Kenichiro,Hauser Michael,Scott Burton,Pericak-Vance Margaret,Vance Jeffery,Martin Eden in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 147-155

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Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

By Svenson Ingrid,Kloos Mark,Gaskell P.,Nance Martha,Garbern James,Hisanaga Shin-ichi,Pericak-Vance Margaret,Ashley-Koch Allison,Marchuk Douglas in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 157-164

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Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey

By Richter Andrea,Ozgul Riza,Poisson Virginie,Topaloglu Haluk in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 165-170

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A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes

By Kleopa Kleopas,Georgiou Domna-Maria,Nicolaou Paschalis,Koutsou Pantelitsa,Papathanasiou Eleftherios,Kyriakides Theodoros,Christodoulou Kyproula in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 171-175

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A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

By Spadaro Maria,Ursu Simona,Lehmann-Horn Frank,Liana Veneziano,Giovanni Antonini,Paola Giunti,Frontali Marina,Jurkat-Rott Karin in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 177-185

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Heterozygous mutation in 5’-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystonia

By Steinberger Daniela,Blau Nenad,Goriuonov Dimitri,Bitsch Juliane,Zuker Michael,Hummel Sibylla,Müller Ulrich in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 187-190

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Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia

By Parrini Elena,Mei Davide,Wright Micheal,Dorn Thomas,Guerrini Renzo in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 191-196

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Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genes

By Kok Cindy,Kennerson Marina,Myers Simon,Nicholson Garth in (2004)

Neurogenetics,volume 5,issue 3 , Vol. 5, Iss. 3, 2004-09 , pp. 197-200

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Total 8 item(s)