I. Järvelä
National Public Health Institute
Department of Human Molecular Genetics
Mannerheimintie 166
00300 Helsinki
Finland
Name/email consistency: high
- 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)
- 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)
- 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)
- Prenatally detected paternal uniparental chromosome 13 isodisomy. Järvelä, I., Savukoski, M., Ammälä, P., von Koskull, H. Prenat. Diagn. (1998)