The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein
In: Human Molecular Genetics, Vol. 21 (2012), No. 18, pp. 4038 - 4048
2012article/chapter in journal
BiologyMedicineFaculty of Medicine » Essen University Hospital » Institute of Human GeneticsScientific institutes » Center of Medical Biotechnology (ZMB)
Related: 1 publication(s)
Title in English:
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein
Author:
Neumann, Lisa
- GND
- 1214304125
- LSF ID
- 16263
- ORCID
- 0000-0003-2973-7869
- Other
- connected with university
- LSF ID
- 12750
- Other
- connected with university
- GND
- 172144035
- LSF ID
- 14406
- ORCID
- 0000-0002-8598-8147
- Other
- connected with university
Year of publication:
2012
Open Access?:
OA Embargo
EVALuna Biblio ID
21433
Web of Science ID
PubMed ID
Scopus ID
Language of text:
English