@article{179e1bc8e4634ac6ba19ffbbe0eee5ab,
title = "NCOR2 is a novel candidate gene for migraine-epilepsy phenotype",
keywords = "Neurological disorder, 12q24, 31, linkage analysis, next-generation sequencing (NGS) technologies, comorbidity, pathophysiology, FAMILIAL HEMIPLEGIC MIGRAINE, RETT-SYNDROME, LINKAGE, IDENTIFICATION, MUTATIONS, RESOURCE, PROGRAM, MECP2, 3112 Neurosciences",
author = "Nuottamo, \{Marjo Eveliina\} and Paavo H{\"a}pp{\"o}l{\"a} and Ville Artto and Heidi Hautakangas and Matti Pirinen and Tero Hiekkalinna and Pekka Ellonen and Maija Lepist{\"o} and Eija H{\"a}m{\"a}l{\"a}inen and Auli Siren and Anna-Elina Lehesjoki and Mikko Kallela and Aarno Palotie and Kaunisto, \{Mari Anneli\} and Maija Wessman",
year = "2022",
month = jun,
doi = "10.1177/03331024211068065",
language = "English",
volume = "42",
pages = "631--644",
journal = "Cephalalgia",
issn = "0333-1024",
publisher = "SAGE Publications Ltd",
number = "7",
}