(Q28295847)

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Specification of the phenotype required for men with monoamine oxidase type A deficiency

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Specification of the phenotype required for men with monoamine oxidase type A deficiency (English)

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1

J Hebebrand

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author name string

B Klug

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2

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language of work or name

English

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publication date

September 1995

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published in

Human Genetics

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volume

96

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issue

3

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page(s)

372-6

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cites work

A critical appraisal of X-linked bipolar illness. Evidence for the assumed mode of inheritance is lacking

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7649563

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12 December 2020

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Evidence found for a possible 'aggression gene'

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7649563

retrieved

12 December 2020

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Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7649563

retrieved

12 December 2020

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A critical analysis of data presented in eight studies favouring X-linkage of bipolar illness with special emphasis on formal genetic aspects

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7649563

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7649563

retrieved

12 December 2020

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Identifiers

DOI

10.1007/BF00210430

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Dimensions Publication ID

1040787173

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PubMed publication ID

7649563

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(Q28295847)

Specification of the phenotype required for men with monoamine oxidase type A deficiency

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