家族性低镁血症伴继发性低钙血症——常染色体遗传还是X连锁遗传？ - Suppr

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超能文献

Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance?

作者信息

Pronicka E, Gruszczyńska B

机构信息

Department of Metabolic Diseases, Memorial Child Health Centre, Warsaw, Poland.

出版信息

J Inherit Metab Dis. 1991;14(3):397-9. doi: 10.1007/BF01811713.

DOI:10.1007/BF01811713

PMID:1770801

Abstract

摘要

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本文引用的文献

Parathyroid hormone secretion and responsiveness to parathyroid hormone in primary hypomagnesemia.

Isr J Med Sci. 1983 Apr;19(4):345-8.

[Magnesium deficiency in children].

Arch Fr Pediatr. 1982 Dec;39(10):837-44.

Primary hypomagnesaemia, an autosomal recessive inherited disease?

Lancet. 1983 Apr 23;1(8330):927. doi: 10.1016/s0140-6736(83)91352-1.

Primary hypomagnesaemia, an X-borne allele?

Lancet. 1983 Mar 26;1(8326 Pt 1):701. doi: 10.1016/s0140-6736(83)91986-4.

Primary infantile hypomagnesaemia; report of two cases and review of literature.

Eur J Pediatr. 1989 Feb;148(5):459-61. doi: 10.1007/BF00595914.

Gene mapping of mineral metabolic disorders.

J Inherit Metab Dis. 1989;12 Suppl 1:231-46. doi: 10.1007/BF01799298.

[Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)].

Monatsschr Kinderheilkd (1902). 1979 Jan;127(1):37-42.

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