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Scottish frequency of the common G985 mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS)

✍ Scribed by M. Dundar; W. G. Lanyon; J. M. Connor

Publisher: Springer
Year: 1993
Tongue: English
Weight: 368 KB
Volume: 16
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf00711516

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