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e-Article

Variants in PRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain
Document Type
Article
Author
Marbach, FelixStoyanov, GeorgiErger, FlorianStratakis, Constantine A.Settas, NikolaosLondon, EdraRosenfeld, Jill A.Torti, ErinHaldeman-Englert, ChadSklirou, EvgeniaKessler, ElenaCeulemans, SophiaNelson, Stanley F.Martinez-Agosto, Julian A.Palmer, Christina G.S.Signer, Rebecca H.Acosta, Maria T.Adam, MargaretAdams, David R.Agrawal, Pankaj B.Alejandro, Mercedes E.Alvey, JustinAmendola, LauraAndrews, AshleyAshley, Euan A.Azamian, Mahshid S.Bacino, Carlos A.Bademci, GuneyBaker, EvaBalasubramanyam, AshokBaldridge, DustinBale, JimBamshad, MichaelBarbouth, DeborahBayrak-Toydemir, PinarBeck, AnitaBeggs, Alan H.Behrens, EdwardBejerano, GillBennett, JimmyBerg-Rood, BeverlyBernstein, Jonathan A.Berry, Gerard T.Bican, AnnaBivona, StephanieBlue, ElizabethBohnsack, JohnBonnenmann, CarstenBonner, DevonBotto, LorenzoBoyd, BrennaBriere, Lauren C.Brokamp, EllyBrown, GabrielleBurke, Elizabeth A.Burrage, Lindsay C.Butte, Manish J.Byers, PeterByrd, William E.Carey, JohnCarrasquillo, OlveenChang, Ta Chen PeterChanprasert, SirisakChao, Hsiao-TuanClark, Gary D.Coakley, Terra R.Cobban, Laurel A.Cogan, Joy D.Coggins, MatthewCole, F. SessionsColley, Heather A.Cooper, Cynthia M.Cope, HeidiCraigen, William J.Crouse, Andrew B.Cunningham, MichaelD’Souza, PrecillaDai, HongzhengDasari, SurendraDavis, JoieDaya, Jyoti G.Deardorff, MatthewDell’Angelica, Esteban C.Dhar, Shweta U.Dipple, KatrinaDoherty, DanielDorrani, NaghmehDoss, Argenia L.Douine, Emilie D.Draper, David D.Duncan, LauraEarl, DawnEckstein, David J.Emrick, Lisa T.Eng, Christine M.Esteves, CeciliaFalk, MarniFernandez, LilianaFerreira, CarlosFieg, Elizabeth L.Findley, Laurie C.Fisher, Paul G.Fogel, Brent L.Forghani, IrmanFresard, LaureGahl, William A.Glass, IanGochuico, BernadetteGodfrey, Rena A.Golden-Grant, KatieGoldman, Alica M.Goldrich, Madison P.Goldstein, David B.Grajewski, AlanaGroden, Catherine A.Gutierrez, IrmaHahn, SihounHamid, RizwanHanchard, Neil A.Hassey, KellyHayes, NicholeHigh, FrancesHing, AnneHisama, Fuki M.Holm, Ingrid A.Hom, JasonHorike-Pyne, MarthaHuang, AldenHuang, YongHuryn, LaryssaIsasi, RosarioJamal, FarihaJarvik, Gail P.Jarvik, JeffreyJayadev, SumanKaraviti, LefkotheaKennedy, JenniferKiley, DanaKohane, Isaac S.Kohler, Jennefer N.Korrick, SusanKozuira, MaryKrakow, DeborahKrasnewich, Donna M.Kravets, ElijahKrier, Joel B.LaMoure, Grace L.Lalani, Seema R.Lam, ByronLam, ChristinaLanpher, Brendan C.Lanza, Ian R.Latham, LeaLeBlanc, KimberlyLee, Brendan H.Lee, HaneLevitt, RoyLewis, Richard A.Lincoln, Sharyn A.Liu, PengfeiLiu, Xue ZhongLongo, NicolaLoo, Sandra K.Loscalzo, JosephMaas, Richard L.MacDowall, JohnMacRae, Calum A.Macnamara, Ellen F.Maduro, Valerie V.Majcherska, Marta M.Mak, Bryan C.Malicdan, May Christine V.Mamounas, Laura A.Manolio, Teri A.Mao, RongMaravilla, KennethMarkello, Thomas C.Marom, RonitMarth, GaborMartin, Beth A.Martin, Martin G.Martinez-Agosto, Julian A.Marwaha, ShrutiMcCauley, JacobMcConkie-Rosell, AllynMcCormack, Colleen E.McCray, Alexa T.McGee, ElisabethMefford, HeatherMerritt, J. LawrenceMight, MatthewMirzaa, GhaydaMorava, EvaMoretti, Paolo M.Moretti, PaoloMosbrook-Davis, DeborahMulvihill, John J.Murdock, David R.Nagy, AnnaNakano-Okuno, MarikoNath, AviNelson, Stanley F.Newman, John H.Nicholas, Sarah K.Nickerson, DeborahNieves-Rodriguez, ShirleyNovacic, DonnaOglesbee, DevinOrengo, James P.Pace, LauraPak, StephenPallais, J. CarlPalmer, Christina G.S.Papp, Jeanette C.Parker, Neil H.Phillips, John A.Posey, Jennifer E.Potocki, LorrainePower, BradleyPusey, Barbara N.Quinlan, AaronRaja, Archana N.Rao, Deepak A.Raskind, WendyRenteria, GeneceeReuter, Chloe M.Rives, LynetteRobertson, Amy K.Rodan, Lance H.Rosenfeld, Jill A.Rosenwasser, NatalieRossignol, FrancisRuzhnikov, MauraSacco, RalphSampson, Jacinda B.Samson, Susan L.Saporta, MarioSchaechter, JudySchedl, TimothySchoch, KellyScott, C. RonScott, Daryl A.Shashi, VandanaShin, JimannSigner, Rebecca H.Silverman, Edwin K.Sinsheimer, Janet S.Sisco, KathySmith, Edward C.Smith, Kevin S.Solem, EmilySolnica-Krezel, LiliannaSolomon, BenSpillmann, Rebecca C.Stoler, Joan M.Sullivan, Jennifer A.Sullivan, KathleenSun, AngelaSutton, ShirleySweetser, David A.Sybert, VirginiaTabor, Holly K.Tan, Amelia L.M.Tan, Queenie K.-G.Tekin, MustafaTelischi, FredThorson, WillaThurm, AudreyTifft, Cynthia J.Toro, CamiloTran, Alyssa A.Tucker, Brianna M.Urv, Tiina K.Vanderver, AdelineVelinder, MattViskochil, DaveVogel, Tiphanie P.Wahl, Colleen E.Walker, MelissaWallace, StephanieWalley, Nicole M.Walsh, Chris A.Wambach, JenniferWan, JijunWang, Lee-kaiWangler, Michael F.Ward, Patricia A.Wegner, DanielWener, MarkWenger, TaraPerry, Katherine WesselingWesterfield, MonteWheeler, Matthew T.Whitlock, JordanWolfe, Lynne A.Woods, Jeremy D.Yamamoto, ShinyaYang, JohnYousef, MuhammadZastrow, Diane B.Zein, WadihZhao, ChunliZuchner, StephanAndrews, Marisa V.Grange, Dorothy K.Willaert, RebeccaPerson, RichardTelegrafi, AidaSievers, AaronLaugsch, MagdalenaTheiß, SusanneCheng, YuZhuLichtarge, OlivierKatsonis, PanagiotisStocco, AmberSchaaf, Christian P.
Source
Genetics in Medicine; August 2021, Vol. 23 Issue: 8 p1465-1473, 9p
Subject
Language
ISSN
10983600; 15300366
Abstract
We characterize the clinical and molecular phenotypes of six unrelated individuals with intellectual disability and autism spectrum disorder who carry heterozygous missense variants of the PRKAR1Bgene, which encodes the R1β subunit of the cyclic AMP-dependent protein kinase A (PKA).