TY  - GEN
AU  - Møller,Lisbeth Birk
AU  - Romstad,Anne
AU  - Paulsen,Marianne
AU  - Hougaard,Pia
AU  - Ormazabal,Aida
AU  - Pineda,Mercé
AU  - Blau,Nenad
AU  - Güttler,Flemming
AU  - Artuch,Rafael
TI  - Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency
SN  - 0197-3851
PY  - 2006///0629
KW  - Brain Diseases, Metabolic, Inborn
KW  - diagnosis
KW  - Child, Preschool
KW  - Female
KW  - Humans
KW  - Muscle Hypotonia
KW  - Mutation
KW  - Polymerase Chain Reaction
KW  - Polymorphism, Genetic
KW  - genetics
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - Tyrosine 3-Monooxygenase
KW  - deficiency
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/pd.1193
ER  -