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Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency

✍ Scribed by A. Boutron; C. Acquaviva; C. Vianey-Saban; P. de Lonlay; H. Ogier de Baulny; N. Guffon; D. Dobbelaere; F. Feillet; F. Labarthe; D. Lamireau; A. Cano; T. Billette de Villemeur; A. Munnich; J.M. Saudubray; D. Rabier; O. Rigal; M. Brivet


Book ID
116989333
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
513 KB
Volume
103
Category
Article
ISSN
1096-7192

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