Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?

BACKGROUND: In the last few years trio‐whole exome sequencing (WES) analysis has demonstrated its potential in obtaining genetic diagnoses even in nonspecific clinical pictures and in atypical presentations of known diseases. Moreover WES allows the detection of variants in multiple genes causing di...

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Detalles Bibliográficos
Autores principales: Pezzani, Lidia, Pezzoli, Laura, Pansa, Alessandra, Facchinetti, Barbara, Marchetti, Daniela, Scatigno, Agnese, Lincesso, Anna R., Perego, Loredana, Pingue, Monica, Pellicioli, Isabella, Migliazza, Lucia, Mangili, Giovanna, Galletti, Lorenzo, Giussani, Ursula, Bonanomi, Ezio, Cereda, Anna, Iascone, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057129/
https://www.ncbi.nlm.nih.gov/pubmed/31943948
http://dx.doi.org/10.1002/mgg3.1064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057129/
https://www.ncbi.nlm.nih.gov/pubmed/31943948
http://dx.doi.org/10.1002/mgg3.1064

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