CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH). (Q46277943)

21 December 2017

title

CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH). (English)

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21 December 2017

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Tingting Sui

1

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21 December 2017

Lin Yuan

2

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21 December 2017

Huan Liu

3

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21 December 2017

Mao Chen

4

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21 December 2017

Jichao Deng

5

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21 December 2017

Yong Wang

6

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21 December 2017

Zhanjun Li

7

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21 December 2017

Liangxue Lai

8

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21 December 2017

publication date

28 April 2016

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21 December 2017

published in

Human Molecular Genetics

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21 December 2017

volume

25

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21 December 2017

page(s)

2661-2671

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21 December 2017

issue

13

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21 December 2017

A clinician's guide to X-linked hypophosphatemia

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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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21 January 2018

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21 January 2018

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21 January 2018

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Anti-FGF-23 neutralizing antibodies ameliorate muscle weakness and decreased spontaneous movement of Hyp mice

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype

21 January 2018

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Adaptations of Goldner's Masson trichrome stain for the study of undecalcified plastic embedded bone

21 January 2018

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Phenotype Presentation of Hypophosphatemic Rickets in Adults

21 January 2018

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21 January 2018

Identifiers

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21 December 2017