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Disappearance of congenital noncompaction in hereditary cobalamin‐C‐deficiency 2.5 years after birth
Author(s) -
Finsterer Josef,
Stöllberger Claudia
Publication year - 2013
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-013-9612-4
Subject(s) - cobalamin , human genetics , medicine , genetics , pediatrics , biology , vitamin b12 , gene