Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families

BACKGROUND: The causes for thousands of individually rare recessive diseases have been discovered since the adoption of next generation sequencing (NGS). Following the molecular diagnosis in older children in a family, parents could use this information to opt for fetal genotyping in subsequent preg...

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Detalles Bibliográficos
Autores principales: Issa, Mahmoud Y., Chechlacz, Zinayida, Stanley, Valentina, George, Renee D., McEvoy-Venneri, Jennifer, Belandres, Denice, Elbendary, Hasnaa M., Gaber, Khaled R., Nabil, Ahmed, Abdel-Hamid, Mohamed S., Zaki, Maha S., Gleeson, Joseph G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218834/
https://www.ncbi.nlm.nih.gov/pubmed/32404165
http://dx.doi.org/10.1186/s12920-020-0714-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218834/
https://www.ncbi.nlm.nih.gov/pubmed/32404165
http://dx.doi.org/10.1186/s12920-020-0714-1

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