Four novel mutations in the Tyrosine Hydroxylase gene in patients with infantile parkinsonism

Annals of Human Genetics

Volumn 64, Issue 1, 2000, Pages 25-31

  Swaans, R J M ^a   Rondot, P ^b   Renier, W O ^a   Van Den Heuvel, L P W J ^a   Steenbergen Spanjers, G C H ^a   Wevers, R A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA; PROTEIN; RESTRICTION ENDONUCLEASE; TYROSINE 3 MONOOXYGENASE;

ADULT; ARTICLE; CASE REPORT; CONTROLLED STUDY; DNA SEQUENCE; ENZYME ACTIVE SITE; HUMAN; MALE; MISSENSE MUTATION; PARKINSONISM; PRIORITY JOURNAL; RESTRICTION MAPPING;

ADULT; AMINO ACID SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; EXONS; FEMALE; HUMANS; INTRONS; LEVODOPA; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PARKINSONIAN DISORDERS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE HOMOLOGY, AMINO ACID; TYROSINE 3-MONOOXYGENASE;

EID: 0034110552     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480000007922     Document Type: Article

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