Exome sequencing identifies novel compound heterozygous mutations in GJB3 gene that cause erythrokeratodermia variabilis et progressiva

Detalles Bibliográficos
Autores principales: Deng, Yongqiong, Wang, Hong, Mou, Yunzhu, Zeng, Qi, Xiong, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Research Letters
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585696/
https://www.ncbi.nlm.nih.gov/pubmed/29992552
http://dx.doi.org/10.1111/ajd.12887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585696/
https://www.ncbi.nlm.nih.gov/pubmed/29992552
http://dx.doi.org/10.1111/ajd.12887

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