An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutation

BACKGROUND: The neuronal ceroid lipofuscinoses (NCLs, or Batten disease) comprise the most common Mendelian form of childhood-onset neurodegeneration, but the functions of the known underlying gene products remain poorly understood. The clinical heterogeneity of these disorders may shed light on gen...

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Detalles Bibliográficos
Autores principales: Staropoli, John F, Xin, Winnie, Barone, Rosemary, Cotman, Susan L, Sims, Katherine B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443422/
https://www.ncbi.nlm.nih.gov/pubmed/22727047
http://dx.doi.org/10.1186/1471-2350-13-50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443422/
https://www.ncbi.nlm.nih.gov/pubmed/22727047
http://dx.doi.org/10.1186/1471-2350-13-50

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