Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency

We add two novel variants to the existing mutation spectrum of ASNS gene. Loss of ASNS function should be suspected in newborns presenting with congenital microcephaly, intellectual disability, progressive cerebral atrophy, and intractable seizures. Acquisition and sequencing of stored newborn blood...

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Detalles Bibliográficos
Autores principales: Abhyankar, Avinash, Lamendola‐Essel, Michelle, Brennan, Kelly, Giordano, Jessica L., Esteves, Cecilia, Felice, Vanessa, Wapner, Ronald, Jobanputra, Vaidehi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771929/
https://www.ncbi.nlm.nih.gov/pubmed/29375865
http://dx.doi.org/10.1002/ccr3.1284

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771929/
https://www.ncbi.nlm.nih.gov/pubmed/29375865
http://dx.doi.org/10.1002/ccr3.1284

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