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. 2000 Jun;23(4):341-4.

doi: 10.1023/a:1005670911799.

3-Methylglutaconyl-CoA hydratase deficiency: a new patient with speech retardation as the leading sign

R Ensenauer¹, C B Müller, K O Schwab, K M Gibson, M Brandis, W Lehnert

Affiliations

PMID: 10896289
DOI: 10.1023/a:1005670911799

3-Methylglutaconyl-CoA hydratase deficiency: a new patient with speech retardation as the leading sign

R Ensenauer et al. J Inherit Metab Dis. 2000 Jun.

. 2000 Jun;23(4):341-4.

doi: 10.1023/a:1005670911799.

Authors

R Ensenauer¹, C B Müller, K O Schwab, K M Gibson, M Brandis, W Lehnert

Affiliation

¹ University Children's Hospital Freiburg, Germany.

PMID: 10896289
DOI: 10.1023/a:1005670911799

No abstract available

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References

1. J Pediatr. 1982 Oct;101(4):551-4 - PubMed
1. J Inherit Metab Dis. 1999 Feb;22(1):1-8 - PubMed
1. Eur J Pediatr. 1994;153(7 Suppl 1):S9-13 - PubMed
1. J Inherit Metab Dis. 1995;18(5):645-6 - PubMed
1. Clin Chim Acta. 1989 Sep 15;184(1):57-64 - PubMed

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