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Familial hypomagnesaemia with secondary hypocalcaemia: a new case that indicates autosomal recessive inheritance
1Institute of Human Genetics, University of Heidelberg, Germany. peter.meyer@med.uni-tuebingen.de
Journal of Inherited Metabolic Disease
|March 28, 2002
Abstract:
Male and female siblings, now aged 18 and 23 years respectively, with familial hypomagnesaemia and secondary hypocalcaemia provide further evidence that this is an autosomal recessive disorder and not X-linked as originally thought.