The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein.
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| Title: | The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. |
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| Authors: | Neumann LC; Institut für Humangenetik, Universitätsklinikum Essen, D-45122 Essen, Germany., Markaki Y, Mladenov E, Hoffmann D, Buiting K, Horsthemke B |
| Source: | Human molecular genetics [Hum Mol Genet] 2012 Sep 15; Vol. 21 (18), pp. 4038-48. Date of Electronic Publication: 2012 Jun 13. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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