Bibliographic Details
| Title: |
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. |
| 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 |
