Identification of a British cohort of patients with a phenotype similar to that found to be associated with a premature stop codon in the monoamine oxidase A (MAOA) gene

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 81, Issue 6, 1998, Pages 467-468

  Stamps, R ^b   Gurling, H M D ^b   Abeling, N G G M ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b NONE

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EID: 0342511498     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: None     Document Type: Article

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