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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

I. Järvelä

National Public Health Institute

Department of Human Molecular Genetics

Mannerheimintie 166

00300 Helsinki

Finland

[email]@ktl.fi

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • National Public Health Institute, Department of Human Molecular Genetics, Mannerheimintie 166, 00300 Helsinki, Finland. 1998 - 1999
  • Department of Human Molecular Genetics, National Public Health Institute, Finland. 1998
  • Department of Obstetrics and Gynaecology, Helsinki University Hospital, Finland. 1998

References

  1. Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL). Järvelä, I., Lehtovirta, M., Tikkanen, R., Kyttälä, A., Jalanko, A. Hum. Mol. Genet. (1999) [Pubmed]
  2. Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease. Järvelä, I., Sainio, M., Rantamäki, T., Olkkonen, V.M., Carpén, O., Peltonen, L., Jalanko, A. Hum. Mol. Genet. (1998) [Pubmed]
  3. Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene. Järvelä, I., Enattah, N.S., Kokkonen, J., Varilo, T., Savilahti, E., Peltonen, L. Am. J. Hum. Genet. (1998) [Pubmed]
  4. Prenatally detected paternal uniparental chromosome 13 isodisomy. Järvelä, I., Savukoski, M., Ammälä, P., von Koskull, H. Prenat. Diagn. (1998) [Pubmed]
 
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