(Q48049188)

8 February 2018

title

Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets (English)

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8 February 2018

author

Fiona Francis

1

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8 February 2018

Thomas Meitinger

17

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8 February 2018

Hans Lehrach

18

object named as

Lehrach H

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8 February 2018

Strom TM

2

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8 February 2018

Hennig S

3

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8 February 2018

Böddrich A

4

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Lorenz B

5

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Brandau O

6

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8 February 2018

Mohnike KL

7

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8 February 2018

Cagnoli M

8

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8 February 2018

Steffens C

9

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8 February 2018

Klages S

10

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8 February 2018

Borzym K

11

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Pohl T

12

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8 February 2018

Oudet C

13

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8 February 2018

Econs MJ

14

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8 February 2018

Rowe PS

15

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8 February 2018

Reinhardt R

16

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publication date

1 June 1997

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8 February 2018

published in

Genome Research

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8 February 2018

volume

7

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8 February 2018

issue

6

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8 February 2018

page(s)

573-585

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8 February 2018

Basic local alignment search tool

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cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone

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Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets

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A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

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The role of introns in evolution

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Molecular characterization of human and bovine endothelin converting enzyme (ECE-1)

21 January 2018

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Predicting internal exons by oligonucleotide composition and discriminant analysis of spliceable open reading frames

21 January 2018

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21 January 2018

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21 January 2018

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Split-gene evolution: Exon shuffling and intron insertion in serine protease genes

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21 January 2018

Identifiers

DOI

10.1101/GR.7.6.573

1 reference

8 February 2018

release_mtyo2lk5zvaevnpororawfmqeq

Fatcat ID

0 references

1 reference

8 February 2018