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A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)

✍ Scribed by R. A. Wevers; J. F. de Rijk-van Andel; C. Bräutigam; B. Geurtz; L. P. W. J. van den Heuvel; G. C. H. Steenbergen-Spanjers; J. A. M. Smeitink; G. F. Hoffmann; F. J. M. Gabreëls

Book ID: 110225675
Publisher: Springer
Year: 1999
Tongue: English
Weight: 96 KB
Volume: 22
Category: Article
ISSN: 0141-8955
DOI: 10.1023/a:1005539803576

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