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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype

✍ Scribed by L. Ijlst; S. Uskikubo; T. Kamijo; T. Hashimoto; J. P. N. Ruiter; J. B. C. Klerk; R. J. A. Wanders

Publisher: Springer
Year: 1995
Tongue: English
Weight: 222 KB
Volume: 18
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf00711778

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