Double homozygosity for mutations of AGL and SCN9A mimicking neurohepatopathy syndrome. | Neurology;70(24): 2343-4, 2008 Jun 10. | MEDLINE

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Double homozygosity for mutations of AGL and SCN9A mimicking neurohepatopathy syndrome.

Ebermann, I; Elsayed, S M; Abdel-Ghaffar, T Y; Nürnberg, G; Nürnberg, P; Elsobky, E; Bolz, H J.

Affiliation

Ebermann I; Institute of Human Genetics, University of Cologne, Cologne, Germany.

Neurology ; 70(24): 2343-4, 2008 Jun 10.

Article in En | MEDLINE | ID: mdl-18541889

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sodium Channels / Pain Insensitivity, Congenital / Homozygote / Mutation Type of study: Diagnostic_studies Limits: Child / Female / Humans / Infant / Male Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sodium Channels / Pain Insensitivity, Congenital / Homozygote / Mutation Type of study: Diagnostic_studies Limits: Child / Female / Humans / Infant / Male Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Country of publication: