A Functional Polymorphism in the Tyrosine Hydroxylase Gene Indicates a Role of Noradrenalinergic Signaling in Sudden Infant Death Syndrome
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Supported by grant 12054 of the Jubilee Fund of the ÖNB.
PII: S0022-3476(08)00115-7
doi:10.1016/j.jpeds.2008.02.032
© 2008 Mosby, Inc. All rights reserved.
