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Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

American Journal of Human Genetics - United States
doi 10.1016/j.ajhg.2019.03.022
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Abstract

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Categories
Genetics
Date

May 1, 2019

Authors
Scott BellJustine RousseauHuashan PengZahia AouabedPierre PriamJean-Francois TherouxMalvin JefriArnaud TantiHanrong WuIlaria KolobovaHeika SilvieraKarla Manzano-VargasSophie EhresmannFadi F. HamdanNuwan HettigeXin ZhangLilit AntonyanChristina NassifLina Ghaloul-GonzalezJessica SebastianJerry VockleyAmber G. BegtrupIngrid M. WentzensenAmy CrunkRobert D. NichollsKristin C. HermanJoshua L. DeignanWalla Al-HertaniStephanie EfthymiouVincenzo SalpietroNoriko MiyakeYoshio MakitaNaomichi MatsumotoRune ØsternGunnar HougeMaria HafströmEmily FassiHenry HouldenJolien S. Klein Wassink-RuiterDominic NelsonAmy GoldsteinTabib DabirJulien van GilsThomas BourgeronRichard DelormeGregory M. CooperJose E. MartinezCandice R. FinnilaLionel CarmantAnne LortieRenske OegemaKoen van GassenSarju G. MehtaDagmar HuhleRami Abou JamraSonja MartinHan G. BrunnerDick LindhoutMargaret AuJohn M. GrahamChristine CoubesGustavo TureckiSimon GravelNaguib MechawarElsa RossignolJacques L. MichaudJulie LessardCarl ErnstPhilippe M. Campeau
Publisher

Elsevier BV

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