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major intrinsically disordered Notch2-binding receptor 1 isoform X1 [Homo sapiens]

NCBI Reference Sequence: XP_054233541.1

GenPept Identical Proteins FASTA 

Supplemental Content

Reference sequence information

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  • retinol dehydrogenase 13 isoform X2 [Homo sapiens]
    retinol dehydrogenase 13 isoform X2 [Homo sapiens]
    gi|2462501700|ref|XP_054189591.1|
    Protein
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    Tourette Syndrome
    A neuropsychological disorder related to alterations in DOPAMINE metabolism and neurotransmission involving frontal-subcortical neuronal circuits. Both multiple motor and one ...<br/>Year introduced: 1989(1966)
    MeSH

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