Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease – a new type of neuronal ceroid lipofuscinosis (CLN15)?

Homozygous mutation of TBC1 domain-containing kinase (TBCK) is the cause of a very recently defined severe childhood disorder, which is characterized by severe hypotonia, global developmental delay, intellectual disability, epilepsy, characteristic facies and premature death. The link between TBCK l...

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Detalles Bibliográficos
Autores principales: Beck-Wödl, Stefanie, Harzer, Klaus, Sturm, Marc, Buchert, Rebecca, Rieß, Olaf, Mennel, Hans-Dieter, Latta, Elisabeth, Pagenstecher, Axel, Keber, Ursula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307319/
https://www.ncbi.nlm.nih.gov/pubmed/30591081
http://dx.doi.org/10.1186/s40478-018-0646-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307319/
https://www.ncbi.nlm.nih.gov/pubmed/30591081
http://dx.doi.org/10.1186/s40478-018-0646-6

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