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Details on Person Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome
| Class:Id | LiteratureReference:5682276 |
|---|---|
| _displayName | Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome |
| _timestamp | 2015-03-06 10:24:47 |
| author | [Person:5682273] Lapicka-Bodzioch, K [Person:5682237] Bodzioch, M [Person:5682207] Krüll, M [Person:5682225] Kielar, D [Person:5682212] Probst, M [Person:5682213] Kiec, B [Person:5682247] Andrikovics, H [Person:5682226] Böttcher, A [Person:5682208] Hubacek, J [Person:5682263] Aslanidis, C [Person:5682279] Suttorp, N [Person:5682257] Schmitz, G |
| created | [InstanceEdit:5682221] Jassal, Bijay, 2015-03-06 |
| journal | Biochim. Biophys. Acta |
| pages | 42-8 |
| pubMedIdentifier | 11476961 |
| title | Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome |
| volume | 1537 |
| year | 2001 |
| (literatureReference) | [FailedReaction:5682111] Defective ABCA1 does not transport CHOL from transport vesicle membrane to plasma membrane [Homo sapiens] |
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No pathways have been reviewed or authored by Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome (5682276)
