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3-Methylcrotonyl-CoA carboxylase deficiency: Mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening
Maria Fernanda Dantas, Terttu Suormala, Ann Randolph, David Coelho, Brian Fowler, David Valle, Matthias R. BaumgartnerVolume:
26
Année:
2005
Langue:
english
Pages:
1
DOI:
10.1002/humu.9352
Fichier:
PDF, 246 KB
english, 2005