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008 140121s2014 gw | s |||| 0|eng d
020 _a9783319034614
024 7 _a10.1007/978-3-319-03461-4
_2doi
040 _dES-MaUEC
050 4 _aRC627.8
_bJ563 2014
245 0 0 _aJIMD Reports
_nVolume 12
_cedited by Johannes Zschocke, K Michael Gibson, Garry Brown, Eva Morava, Verena Peters.
260 _aCham, Switzerland
_bSpringer International Publishing
_c2014
300 _a1 recurso en línea (VI, 134 p.)
_b90 ilustraciones, 17 ilustraciones en color
336 _aTexto (visual)
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 0 _aJIMD Reports
_x2192-8304
_v12
520 _aJIMD 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.
650 7 _2embne
_9156016
_aEnfermedades hereditarias metabólicas
700 1 _aZschocke, Johannes
_eeditor literario
_933188
_0comprobar BNE20012548357
700 1 _aGibson, K. Michael
_eeditor literario
_0Local
_988505
700 1 _aBrown, Garry
_eeditor literario
_988506
_0Local
700 1 _aMorava, Eva
_eeditor literario
_988507
_0Local
700 1 _aPeters, Verena
_eeditor literario
_988508
_0Local
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-03461-4
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
907 _a.b12881387
_b10-10-17
_c11-11-15
942 _2lcc
_cLE
945 _aRC627.8 J563 2014 EB
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