1. Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype

   • Sofia A. Oliveira
   • William K. Scott
   • Eden R. Martin

   Original Article 08 June 2004 Pages: 147 - 155

   

2. Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

   • Ingrid K. Svenson
   • Mark T. Kloos
   • Douglas A. Marchuk

   Original Article 10 July 2004 Pages: 157 - 164

   

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

   • Andrea M. Richter
   • Riza Koksal Ozgul
   • Haluk Topaloglu

   Original Article 20 May 2004 Pages: 165 - 170

   

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

   • Kleopas A. Kleopa
   • Domna-Maria Georgiou
   • Kyproula Christodoulou

   Original Article 17 June 2004 Pages: 171 - 175

   

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

   • Maria Spadaro
   • Simona Ursu
   • Karin Jurkat-Rott

   Original Article 31 July 2004 Pages: 177 - 185

   

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

   • Daniela Steinberger
   • Nenad Blau
   • Ulrich Müller

   Original Article 06 July 2004 Pages: 187 - 190

   

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

   • Elena Parrini
   • Davide Mei
   • Renzo Guerrini

   Short Communication 28 July 2004 Pages: 191 - 196

   

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

   • Cindy Kok
   • Marina L. Kennerson
   • Garth A. Nicholson

   Short Communication 06 July 2004 Pages: 197 - 200