Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C disease: Response to letter “Disappearance of congenital noncompaction in hereditary cobalamin-C-deficiency 2.5 years after birth” by J. Finsterer and Claudia Stöllberger, DOI 10.1007/s10545-013-9612-4

Author: Tanpaiboon Pranoot   Venditti Charles  

Publisher: Springer Publishing Company

ISSN: 0141-8955

Source: Journal of Inherited Metabolic Disease, Vol.36, Iss.6, 2013-11, pp. : 1085-1085

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Abstract