Zeynep Tümer

Clinical Professor

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2003
Published
Cloning, characterization and chromosomal localization of the Sus scrof SLC31A1gene
Harboe, T. L., Jensen, L. R., Hansen, C., Horn, P., Bendixen, C., Tommerup, Niels & Tümer, Asuman Zeynep, 2003, In: Animal Genetics. Vol. 34, p. 59-61
Research output: Contribution to journal › Journal article › Research › peer-review
Published
Menkes disease
Tümer, Asuman Zeynep & Horn, N., 2003, Neurocutaneous disorders. UK: Cambridge University Press, p. 222-233
Research output: Chapter in Book/Report/Conference proceeding › Report chapter › Research
Published
Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7A
Tümer, Asuman Zeynep, Møller, L. B. & Horn, L., 2003, In: Hum. Mutat.. Vol. 22, p. 457-464
Research output: Contribution to journal › Journal article › Research › peer-review

ID: 7071

2602 downloads
Dysfunction of the heteromeric K_V7.3/K_V7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
Published
1859 downloads
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
Published
1136 downloads
Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans
Research output: Contribution to journal › Journal article › Research › peer-review
Published