Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients-Reference-Cited by-同舟云学术

Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients

Published:2010-07 Issue:7-8 Volume:1802 Page:639-648
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

van Kuilenburg André B.P.,Dobritzsch Doreen,Meijer Judith,Meinsma Rutger,Benoist Jean-François,Assmann Birgit,Schubert Susanne,Hoffmann Georg F.,Duran Marinus,de Vries Maaike C.,Kurlemann Gerd,Eyskens François J.M.,Greed Lawrence,Sass Jörn Oliver,Schwab K. Otfried,Sewell Adrian C.,Walter John,Hahn Andreas,Zoetekouw Lida,Ribes Antonia,Lind Suzanne,Hennekam Raoul C.M.

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference61 articles.

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