Familial hypomagnesaemia with secondary hypocalcaemia: A new case that indicates autosomal recessive inheritance

被引:4
作者
Meyer, P
Boettger, MB
机构
[1] Univ Heidelberg, Inst Human Genet, Heidelberg, Germany
[2] Human Resources Inc, Tubingen, Germany
关键词
D O I
10.1023/A:1013952510698
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:875 / 876
页数:2
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