CS16-7. A novel autosomal recessive and autosomal dominant deficiency in the TLR3 pathway underlying susceptibility to Herpes Simplex Encephalitis

Vanessa Sancho Shimizu; Rebeca Perez; Lazaro Lorenzo; Rabih Halwani; Sylvie Fabrega; Annabelle Cardon; Laurent Abel; ShenYing Zhang; Anne Puel; Saleh Al-Muhsen; Jean Laurent Casanova

doi:10.1016/j.cyto.2011.07.412

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CS16-7. A novel autosomal recessive and autosomal dominant deficiency in the TLR3 pathway underlying susceptibility to Herpes Simplex Encephalitis

Journal article

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CS16-7. A novel autosomal recessive and autosomal dominant deficiency in the TLR3 pathway underlying susceptibility to Herpes Simplex Encephalitis

Vanessa Sancho Shimizu, Rebeca Perez, Lazaro Lorenzo, Rabih Halwani, Sylvie Fabrega, Annabelle Cardon, Laurent Abel, ShenYing Zhang, Anne Puel, Saleh Al-Muhsen, …

Cytokine (Philadelphia, Pa.), Vol.56(1), pp.106-106

01/10/2011

DOI: https://doi.org/10.1016/j.cyto.2011.07.412

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Title: CS16-7. A novel autosomal recessive and autosomal dominant deficiency in the TLR3 pathway underlying susceptibility to Herpes Simplex Encephalitis
Creators - without role: Vanessa Sancho Shimizu - Institute of Human Genetics
Rebeca Perez - Institute of Human Genetics
Lazaro Lorenzo - Inserm
Rabih Halwani - King Saud University
Sylvie Fabrega - Institut Necker Enfants Malades
Annabelle Cardon - Institute of Human Genetics
Laurent Abel - Institute of Human Genetics
ShenYing Zhang - Rockefeller University
Anne Puel - Inserm
Saleh Al-Muhsen - King Saud University
Jean Laurent Casanova - Institute of Human Genetics
Publication Details: Cytokine (Philadelphia, Pa.), Vol.56(1), pp.106-106
Publisher: Elsevier Ltd
Identifiers: 9946577908331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article