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5 results for author:"Westermark K." in Literature citations

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Psychopathology and personality traits in patients with treated Wilson disease grouped according to gene mutations.

Portala K., Waldenstrom E., von Knorring L., Westermark K.

Ups. J. Med. Sci. 113:79-94(2008) · Mapped (9)

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

Shah A.B., Chernov I., Zhang H.T., Ross B.M., Das K., Lutsenko S., Parano E., Pavone L., Evgrafov O., Ivanova-Smolenskaya I.A. et al.

Am. J. Hum. Genet. 61:317-328(1997) · UniProtKB (1)

Efficient detection of mutations in Wilson disease by manifold sequencing.

Waldenstroem E., Lagerkvist A., Dahlman T., Westermark K., Landegren U.

Genomics 37:303-309(1996) · UniProtKB (1)

Functional analysis of a variant of the thyrotropin receptor gene in a family with Graves' disease.

Gustavsson B., Eklof C., Westermark K., Westermark B., Heldin N.-E.

Mol. Cell. Endocrinol. 111:167-173(1995) · UniProtKB (1)

A somatic point mutation in a putative ligand binding domain of the TSH receptor in a patient with autoimmune hyperthyroidism.

Heldin N.-E., Gustavsson B., Westermark K., Westermark B.

J. Clin. Endocrinol. Metab. 73:1374-1376(1991) · UniProtKB (1)

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