Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)-Reference-Cited by-同舟云学术

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Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)

Published:1997-04-01 Issue:4 Volume:6 Page:539-549
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Rowe P.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Cited by 183 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sclerostin inhibition in rare bone diseases: Molecular understanding and therapeutic perspectives;Journal of Orthopaedic Translation;2024-07

2. Three exonic variants in the PHEX gene cause aberrant splicing in a minigene assay;Frontiers in Genetics;2024-05-22

3. Clinical disorders of phosphate homeostasis;Feldman and Pike's Vitamin D;2024

4. A PAI‐1 antagonist ameliorates hypophosphatemia in the Hyp vitamin D‐resistant rickets model mouse;FEBS Open Bio;2023-12-25

5. Whole exome sequencing identifies two novel variants in PHEX and DMP1 in Malaysian children with hypophosphatemic rickets;Italian Journal of Pediatrics;2022-12-08

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