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Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder.
D'Onofrio G, Accogli A, Severino M, Caliskan H, Kokotović T, Blazekovic A, Jercic KG, Markovic S, Zigman T, Goran K, Barišić N, Duranovic V, Ban A, Borovecki F, Ramadža DP, Barić I, Fazeli W, Herkenrath P, Marini C, Vittorini R, Gowda V, Bouman A, Rocca C, Alkhawaja IA, Murtaza BN, Rehman MMU, Al Alam C, Nader G, Mancardi MM, Giacomini T, Srivastava S, Alvi JR, Tomoum H, Matricardi S, Iacomino M, Riva A, Scala M, Madia F, Pistorio A, Salpietro V, Minetti C, Rivière JB, Srour M, Efthymiou S, Maroofian R, Houlden H, Vernes SC, Zara F, Striano P, Nagy V. D'Onofrio G, et al. Among authors: vernes sc. Hum Genet. 2023 Jul;142(7):909-925. doi: 10.1007/s00439-023-02552-2. Epub 2023 May 14. Hum Genet. 2023. PMID: 37183190 Free PMC article. Review.
Shining a light on CNTNAP2: complex functions to complex disorders.
Rodenas-Cuadrado P, Ho J, Vernes SC. Rodenas-Cuadrado P, et al. Among authors: vernes sc. Eur J Hum Genet. 2014 Feb;22(2):171-8. doi: 10.1038/ejhg.2013.100. Epub 2013 May 29. Eur J Hum Genet. 2014. PMID: 23714751 Free PMC article. Review.
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants.
Scala M, Anijs M, Battini R, Madia F, Capra V, Scudieri P, Verrotti A, Zara F, Minetti C, Vernes SC, Striano P. Scala M, et al. Among authors: vernes sc. Ital J Pediatr. 2021 Oct 12;47(1):208. doi: 10.1186/s13052-021-01162-w. Ital J Pediatr. 2021. PMID: 34641913 Free PMC article.
61 results