Associated Papers
Genetics of catatonia: a systematic review of case reports and a gene pathway analysis.
Moyal M et al.
European Psychiatry : the Journal of the Association of European Psychiatrists, 2025
Catatonia in Children and Adolescents: A High Rate of Genetic Conditions.
Raffin M et al.
Journal of the American Academy of Child and Adolescent Psychiatry, 2018
Long-term neuropsychiatric follow-up in hyperprolinemia type I.
Di Rosa G et al.
Psychiatric Genetics, 2014
Type I hyperprolinemia: genotype/phenotype correlations.
Guilmatre A et al.
Human Mutation, 2010
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Raux G et al.
Human Molecular Genetics, 2007
Functional consequences of PRODH missense mutations.
Bender HU et al.
American Journal of Human Genetics, 2005
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