Login
- Dokumenttyp:
- Editorial Material; Journal Article; Comment
- Autor(en):
- Oexle, Konrad; Winkelmann, Juliane
- Titel:
- Common Grounds for Family Maladies.
- Abstract:
- Rare variants cause Mendelian family aggregation in subsets of common diseases, and common variants may contribute to rare diseases. In this issue of Neuron, Gormley et al. (2018) report that the common variant burden in familial migraine is larger than in migraine of the general population.
- Zeitschriftentitel:
- Neuron
- Jahr:
- 2018
- Band / Volume:
- 98
- Heft / Issue:
- 4
- Seitenangaben Beitrag:
- 671-672
- Volltext / DOI:
- doi:10.1016/j.neuron.2018.05.006
- PubMed:
- http://view.ncbi.nlm.nih.gov/pubmed/29772195
- Print-ISSN:
- 0896-6273
- TUM Einrichtung:
- Institut für Humangenetik; Lehrstuhl für Neurogenetik (Prof. Winkelmann)
BibTeX