The topology, structure and PE interaction of LITAF underpin a Charcot-Marie-Tooth disease type 1C

BACKGROUND: Mutations in Lipopolysaccharide-induced tumour necrosis factor-α factor (LITAF) cause the autosomal dominant inherited peripheral neuropathy, Charcot-Marie-Tooth disease type 1C (CMT1C). LITAF encodes a 17 kDa protein containing an N-terminal proline-rich region followed by an evolutiona...

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Detalles Bibliográficos
Autores principales: Ho, Anita K., Wagstaff, Jane L., Manna, Paul T., Wartosch, Lena, Qamar, Seema, Garman, Elspeth F., Freund, Stefan M. V., Roberts, Rhys C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142333/
https://www.ncbi.nlm.nih.gov/pubmed/27927196
http://dx.doi.org/10.1186/s12915-016-0332-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5142333/
https://www.ncbi.nlm.nih.gov/pubmed/27927196
http://dx.doi.org/10.1186/s12915-016-0332-8

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