Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2

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Detalles Bibliográficos
Autores principales: Jepsen, Wayne M., Ramsey, Keri, Szelinger, Szabolcs, Llaci, Lorida, Balak, Chris, Belnap, Newell, Bilagody, Cherae, De Both, Matthew, Gupta, Raj, Naymik, Marcus, Pandey, Richa, Piras, Ignazio S., Sanchez‐Castillo, Meredith, Rangasamy, Sampathkumar, Narayanan, Vinodh, Huentelman, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852257/
https://www.ncbi.nlm.nih.gov/pubmed/31236915
http://dx.doi.org/10.1111/cge.13580

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852257/
https://www.ncbi.nlm.nih.gov/pubmed/31236915
http://dx.doi.org/10.1111/cge.13580

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