Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

Author:

Henden Lyndal,Freytag Saskia,Afawi Zaid,Baldassari Sara,Berkovic Samuel F.,Bisulli Francesca,Canafoglia Laura,Casari Giorgio,Crompton Douglas Ewan,Depienne Christel,Gecz Jozef,Guerrini Renzo,Helbig Ingo,Hirsch Edouard,Keren Boris,Klein Karl Martin,Labauge Pierre,LeGuern Eric,Licchetta Laura,Mei Davide,Nava Caroline,Pippucci Tommaso,Rudolf Gabrielle,Scheffer Ingrid Eileen,Striano Pasquale,Tinuper Paolo,Zara Federico,Corbett Mark,Bahlo Melanie

Funder

National Health and Medical Research Council Program Grant

National Health and Medical Research Council Senior Research Fellowship

The John and Patricia Farrant Scholarship

The Australian Postgraduate Award Scholarship

Victorian State Government Operational Infrastructure Support

Australian Government National Health and Medical Research Council Independent Research Institute Infrastructure Support Scheme

Fondation Maladies rares

Assistance Publique des Hôpitaux de Paris

Université Pierre et Marie-Curie

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

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