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Title:

Common Grounds for Family Maladies.

Document type:
Editorial Material; Journal Article; Comment
Author(s):
Oexle, Konrad; Winkelmann, Juliane
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.
Journal title abbreviation:
Neuron
Year:
2018
Journal volume:
98
Journal issue:
4
Pages contribution:
671-672
Fulltext / DOI:
doi:10.1016/j.neuron.2018.05.006
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/29772195
Print-ISSN:
0896-6273
TUM Institution:
Institut für Humangenetik; Lehrstuhl für Neurogenetik (Prof. Winkelmann)
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