Activation of an exonic splice‐donor site in exon 30 of CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalities

This report constitutes the first report of a cryptic exonic splice‐donor site in CDK5RAP2, highlights the importance of evaluating novel splice mutations, and suggests that the phenotypic range associated with CDK5RAP2 mutations may include skin pigmentary abnormalities.

Detalles Bibliográficos
Autores principales: Pagnamenta, Alistair T., Howard, Malcolm F., Knight, Samantha J. L., Keays, David A., Quaghebeur, Gerardine, Taylor, Jenny C., Kini, Usha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054469/
https://www.ncbi.nlm.nih.gov/pubmed/27761245
http://dx.doi.org/10.1002/ccr3.663

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054469/
https://www.ncbi.nlm.nih.gov/pubmed/27761245
http://dx.doi.org/10.1002/ccr3.663

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