J Müller-Höcker

Copper storage disease of the liver and chronic dietary copper intoxication in two further German infants mimicking Indian childhood cirrhosis.

P Schramel, P. Schramel, J. Müller‐Höcker, 1988, Pathology, research and practice.

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

H. Goebel, H. Lochmüller, F. Rüschendorf, 2004, Journal of Medical Genetics.

Expression of glucose transporter 1 in human endometrial and decidual tissue

E. Capp, T. Strowitzki, M. von Wolff, 2001, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.