L-2-hydroxyglutaric aciduria: characterisation of the molecular defect in a spontaneous canine model. | J Med Genet;44(5): 334-40, 2007 May. | MEDLINE

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L-2-hydroxyglutaric aciduria: characterisation of the molecular defect in a spontaneous canine model.

Penderis, Jacques; Calvin, Jacqui; Abramson, Carley; Jakobs, Cornelis; Pettitt, Louise; Binns, Matthew M; Verhoeven, Nanda M; O'Driscoll, Eamonn; Platt, Simon R; Mellersh, Cathryn S.

J Med Genet ; 44(5): 334-40, 2007 May.

Article in En | MEDLINE | ID: mdl-17475916

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dog Diseases / Amino Acid Metabolism, Inborn Errors / Glutarates Type of study: Diagnostic_studies Limits: Animals Language: En Journal: J Med Genet Year: 2007 Document type: Article Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dog Diseases / Amino Acid Metabolism, Inborn Errors / Glutarates Type of study: Diagnostic_studies Limits: Animals Language: En Journal: J Med Genet Year: 2007 Document type: Article Country of publication: