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020 _a9783662467008
024 7 _a10.1007/978-3-662-46700-8
_2doi
050 4 _aRC627.8
_b2015 EB
082 0 4 _a611.01816
082 0 4 _a599.935
245 0 0 _aJIMD Reports
_nVolume 20
_cedited by Johannes Zschocke, Matthias Baumgartner, Eva Morava, Marc Patterson, Shamima Rahman, Verena Peters
260 _aBerlin, Heidelberg
_bSpringer
_c2015
300 _a1 recurso en línea (VI, 120 p.)
_b28 ilustraciones, 10 ilustraciones en color
336 _aTexto (visual)
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 1 _aJIMD Reports
_x2192-8304
_v20
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
710 2 _aSpringerLink (Online service)
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942 _2lcc
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650 7 _aEnfermedades hereditarias metabólicas
_9156016
_0comprobar BNE19997299243
_2embne
700 1 _aZschocke, Johannes
_eeditor literario
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_0comprobar BNE20012548357
700 1 _aBaumgartner, Matthias R.
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_0comprobar BNE20001827176
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700 1 _aMorava, Eva
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700 1 _aPatterson, Marc
_eeditor literario
_994072
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700 1 _aRahman, Shamima
_eeditor literario
_994073
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700 1 _aPeters, Verena
_eeditor literario
_988508
_0Local
830 0 _aJIMD Reports
_x2192-8304
_v20
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856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-662-46700-8
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
901 _ai9783662467008
907 _a.b12912190
_b10-10-17
_c10-02-16
988 _aSpringer_Medicine_2015
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