De novo mutations in PURA are associated with hypotonia and developmental delay

PURA is the leading candidate gene responsible for the developmental phenotype in the 5q31.3 microdeletion syndrome. De novo mutations in PURA were recently reported in 15 individuals with developmental features similar to the 5q31.3 microdeletion syndrome. Here we describe six unrelated children wh...

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Detalles Bibliográficos
Autores principales: Tanaka, Akemi J., Bai, Renkui, Cho, Megan T., Anyane-Yeboa, Kwame, Ahimaz, Priyanka, Wilson, Ashley L., Kendall, Fran, Hay, Beverly, Moss, Timothy, Nardini, Monica, Bauer, Mislen, Retterer, Kyle, Juusola, Jane, Chung, Wendy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850890/
https://www.ncbi.nlm.nih.gov/pubmed/27148565
http://dx.doi.org/10.1101/mcs.a000356

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850890/
https://www.ncbi.nlm.nih.gov/pubmed/27148565
http://dx.doi.org/10.1101/mcs.a000356

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