JIMD Reports . Volume 22 / edited by Johannes Zschocke, Matthias Baumgartner, Eva Morava, Marc Patterson, Shamima Rahman, Verena Peters.
Contributor(s): SpringerLink (Online service)
| Zschocke, Johannes, editor literario | Baumgartner, Matthias R., editor literario | Morava, Eva, editor literario | Patterson, Marc, editor literario | Rahman, Shamima, editor literario | Peters, Verena, editor literario
Material type: 
E-bookSeries: JIMD Reports; 2222Publisher: Berlin, Heidelberg : Springer, 2015Description: 1 recurso en línea (VI, 120 p.) : 35 ilustraciones, 17 ilustraciones en color.ISBN: 9783662474532.Subject: Metabolismo -- Trastornos | Metabolismo -- Trastornos | Medicina | Fisiología humana | Fisiología humana | Genética humana | Genética humana | Pediatría | PediatríaDDC classification: 611.01816 | 599.935 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)
Summary: JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
| Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds | |
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LIBRO-E NO PRÉSTAMO
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | RB155-155.8 EB (Browse shelf(Opens below)) | .i11579936 | Acceso electrónico | eBOOK .i11579936 |
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| RB155-155.8 EB Founder mutations in inherited cardiac diseases in the Netherlands | RB155-155.8 EB JIMD Reports Volume 18 | RB155-155.8 EB JIMD Reports Volume 19 | RB155-155.8 EB JIMD Reports Volume 22 | RB155-155.8 EB JIMD Reports Volume 23 | RB155-155.8 QH431 Biostatistics for Human Genetic Epidemiology | RB155-155.8 QH431 Prefoldins: the new chaperones |
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
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