Common Grounds for Family Maladies.

Titel:: Common Grounds for Family Maladies.
Dokumenttyp:: Editorial Material; Journal Article; Comment
Autor(en):: 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.
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)
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