The HHID syndrome of hypertrichosis, hyperkeratosis, abnormal corpus callosum, intellectual disability, and minor anomalies is caused by mutations in ARID1B

Detalles Bibliográficos
Autores principales: Zweier, Markus, Peippo, Maarit M., Pöyhönen, Minna, Kääriäinen, Helena, Begemann, Anaïs, Joset, Pascal, Oneda, Beatrice, Rauch, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Letters
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413807/
https://www.ncbi.nlm.nih.gov/pubmed/28323383
http://dx.doi.org/10.1002/ajmg.a.38143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413807/
https://www.ncbi.nlm.nih.gov/pubmed/28323383
http://dx.doi.org/10.1002/ajmg.a.38143

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