Author:
Gallardo M.Esther,Desviat Lourdes R.,Rodríguez José M.,Esparza-Gordillo Jorge,Pérez-Cerdá Celia,Pérez Belén,Rodríguez-Pombo Pilar,Criado Olga,Sanz Raul,Morton D.Holmes,Gibson K.Michael,Le Thuy P.,Ribes Antonia,de Córdoba Santiago Rodríguez,Ugarte Magdalena,Peñalva Miguel Á.
Subject
Genetics (clinical),Genetics
Reference35 articles.
1. Baumgartner MR, Almashanu S, Suormala T, Obie C, Cole RN, Morton DH, Packman S, Baumgartner ER, Valle D. The molecular basis of human 3-methylcrotonyl CoA carboxylase deficiency. J Clin Invest (in press)
2. Mutation and polymorphism analysis of the human homogentisate 1, 2- dioxygenase gene in alkaptonuria patients;Beltrán-Valero de Bernabé;Am J Hum Genet,1998
3. Disorders of branched chain amino acid and ketoacid metabolism;Chuang,1995
4. Quality control in the discovery, reporting and recording of genomic variation;Cotton;Hum Mutat,2000
5. The molecular basis of alkaptonuria;Fernández-Cañón;Nat Genet,1996
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