Literature DB >> 9389727

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

M J Econs1, P T McEnery, F Lennon, M C Speer.   

Abstract

Autosomal dominant hypophosphatemic rickets (ADHR) is an inherited disorder of isolated renal phosphate wasting, the pathogenesis of which is unknown. We performed a genome-wide linkage study in a large kindred to determine the chromosome location of the ADHR gene. Two-point LOD scores indicate that the gene is linked to the markers D12S314 [Z(theta) = 3.15 at theta = 0.0], vWf [Z(theta) = 5.32 at theta = 0.0], and CD4 [Z(theta) = 3.53 at theta = 0.0]. Moreover, multilocus analysis indicates that the ADHR gene locus is located on chromosome 12p13 in the 18-cM interval between the flanking markers D12S100 and D12S397. These data are the first to establish a chromosomal location for the ADHR locus and to provide a framework map to further localize the gene. Such studies will permit ultimate identification of the ADHR gene and provide further insight into phosphate homeostasis.

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Year:  1997        PMID: 9389727      PMCID: PMC508467          DOI: 10.1172/JCI119809

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  20 in total

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Authors:  M A Levine; P M Smallwood; P T Moen; L J Helman; T G Ahn
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Authors:  J Dausset; H Cann; D Cohen; M Lathrop; J M Lalouel; R White
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Review 4.  Molecular genetics of human salivary proteins and their polymorphisms.

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5.  Estimating the power of a proposed linkage study for a complex genetic trait.

Authors:  L M Ploughman; M Boehnke
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Authors:  P M Conneally; J H Edwards; K K Kidd; J M Lalouel; N E Morton; J Ott; R White
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Authors:  R E Straub; M C Speer; Y Luo; K Rojas; J Overhauser; J Ott; T C Gilliam
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Authors:  M J Econs; D F Barker; M C Speer; M A Pericak-Vance; P R Fain; M K Drezner
Journal:  J Clin Endocrinol Metab       Date:  1992-07       Impact factor: 5.958

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  25 in total

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Review 7.  The Causes of Hypo- and Hyperphosphatemia in Humans.

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