REFERENCES

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Databases:

http://www.ensembl.org

http://www.ncbi.nlm.nih.gov/BLAST/

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?

http://genome.imim.es/datasets/sphuman2003/


Programs:

http://genome.unl.edu/SECISearch.html


Articles:

Moghadaszadeh B; et al.Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome .Nature Genetics, 29(1): 17-8, 2001.

Hatfield, D.L. & Gladyshev, V.N. How Selenium Has Altered Our Understanding of the Genetic Code. (2002) Molecular and Cellular Biology 22, 3565–3576.

Lecture from Roderic Guigo 2005-03-06: http://genome.imim.es/courses/BioinformaticaUPF/T23/

(1) Petit. N, et al. Selenoprotein N: an endoplasmatic reticulum glycoprotein with an early developmental expression pattern. Human Molecular Genetics, Vol.12, Nº9, 1045-1053, 2003

(2) Cabello A, Ricoy-Campo JR. Congenital myopathies. Revista Neurología, Vol.8, 779-86, 2003.

(3) Ferreiro A, et al. Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies. The American Journal of Human Genetics. Vol 71(4), 739-749, 2002.

Kryukov, G et al. Characterization of Mammalian Selenoproteomes Science, Vol 300, Issue 5624, 1439-1443