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No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families
by
McKeane, D.P.
,
Meyer, J.
,
Dobrin, S.E.
,
Melmed, K.M.
,
Ekawardhani, S.
,
Tracy, N.A.
,
Lesch, K.P.
,
Stephan, D.A.
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Schizophrenia research
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Schizophrenia Research
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Adult And Adolescent Clinical Studies
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Biological And Medical Sciences
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Blood Proteins - Genetics
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Catatonia - Ethnology
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Catatonia - Genetics
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Chromosomes, Human, Pair 15 - Genetics
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Dll4
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Dopamine
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European Continental Ancestry Group - Genetics
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Genetic Linkage
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Genetic Predisposition To Disease - Ethnology
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Genetic Predisposition To Disease - Genetics
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Germany - Epidemiology
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Humans
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Intercellular Signaling Peptides And Proteins - Genetics
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Life Sciences & Biomedicine
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Medical Sciences
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Notch4
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Polymorphism, Single Nucleotide
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Polymorphism, Single-Stranded Conformational
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