Literature DB >> 11916323

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

P Meyer1, M B Boettger.   

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.

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Year:  2001        PMID： 11916323     DOI： 10.1023/a:1013952510698

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


  3 in total

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

Authors:  Y M Abdulrazzaq; F C Smigura; G Wettrell
Journal:  Eur J Pediatr       Date:  1989-02       Impact factor: 3.183

2.  Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.

Authors:  R Y Walder; H Shalev; T M Brennan; R Carmi; K Elbedour; D A Scott; A Hanauer; A L Mark; S Patil; E M Stone; V C Sheffield
Journal:  Hum Mol Genet       Date:  1997-09       Impact factor: 6.150

3.  Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.

Authors:  M Chery; V Biancalana; C Philippe; G Malpuech; H Carla; S Gilgenkrantz; J L Mandel; A Hanauer
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132
  3 in total
  1 in total

1.  Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic development.

Authors:  Hao Zhou; David E Clapham
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-26       Impact factor: 11.205
  1 in total

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