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SequencingGenomicsAOU Meyer IRCCS; IRCCS Fondazione Stella MarisIllumina NextSeq 500Homo Sapienshttps://www.ebi.ac.uk/eva/?eva-study=PRJEB74924EVAspeech-language disorder 1, developmental verbal apraxia, developmental apraxia of speech, das, articulatory apraxia, SPCH1, speech-language disorder-1.P130CAS, P130Cas, CAS1, DmelCG2102, l(3)neo33, Materials, Crkas, p120, anon-Pen19, cold antibody hemolytic anemia, P120CAS, Xpo2, XPO2, Gene, das, p19, l(2)k03902, Cistrons, BcDNA:GM09207, BcDNA:LD14270, 2610100P18Rik, CTNND, p120(CTN), anemia, CG2102, Dcas, Genetic Materials, cold antibody disease, TFIID, Cas, CAS, developmental verbal apraxia, EWSR1, SARFH, CRKAS, p120(ctn), Sarfh, Genetic Material, Caz, speech-language disorder-1, AA407533, developmental apraxia of speech, Genetic, cold antibody hemolytic anaemia, speech-language disorder 1, CG13281, cold antibody, cas, CASS1., INSDC_feature:gene, SPCH1, CG3606, pen19, P120CTN, l(3)j1C2, hemolytic, dcas, p120(CAS), DmelCG13281, CSE1, ming, articulatory apraxia, Material, Capts, AI385681, DmelCG3606, p120 catenin, p120(cas), Cistron, Pen19, P19, Cadherin-associated Src substratefalseExpanding the molecular landscape of childhood apraxia of speech: evidence from a single-center experienceIdentification of new pathogenic gene variants associated with childhood apraxia of speech (CAS)2024-04-19PRJEB749249606