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Volumn 13, Issue 8, 2008, Pages 3150-3158
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Congenital prosopagnosia - A common hereditary cognitive dysfunction in humans
a
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Author keywords
Autosomal dominant; Congenital; Face blind; Familial recurrence; Hereditary; Incomplete penetrance; Monogenic; Prosopagnosia
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Indexed keywords
ARTICLE;
BIOLOGICAL MODEL;
COGNITIVE DEFECT;
DOMINANT GENE;
FACE;
FEMALE;
GENETIC PROCEDURES;
GENETICS;
HUMAN;
MALE;
MUTATION;
PATTERN RECOGNITION;
PEDIGREE;
PHENOTYPE;
PROSOPAGNOSIA;
QUESTIONNAIRE;
VISION;
COGNITION DISORDERS;
FACE;
FEMALE;
GENES, DOMINANT;
GENETIC TECHNIQUES;
HUMANS;
MALE;
MODELS, GENETIC;
MUTATION;
PATTERN RECOGNITION, VISUAL;
PEDIGREE;
PHENOTYPE;
PROSOPAGNOSIA;
QUESTIONNAIRES;
VISUAL PERCEPTION;
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EID: 38449088696
PISSN: 27686701
EISSN: 27686698
Source Type: Journal
DOI: 10.2741/2916 Document Type: Review |
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Times cited : (26)
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References (71)
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