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Erratum: Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype
Publication year - 2011
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.23946
Subject(s) - tyrosine hydroxylase , phenotype , gene , tyrosine 3 monooxygenase , genetics , psychology , biology , medicine , enzyme , biochemistry