Novel 5.712 kb mitochondrial DNA deletion in a patient with Pearson syndrome: A case report-Reference-Cited by-同舟云学术

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Novel 5.712 kb mitochondrial DNA deletion in a patient with Pearson syndrome: A case report

Published:2014-12-22 Issue:5 Volume:11 Page:3741-3745
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

PARK JOONHONG,RYU HYEJIN,JANG WOORI,CHAE HYOJIN,KIM MYUNGSHIN,KIM YONGGOO,KIM JIYEON,LEE JAE WOOK,CHUNG NACK-GYUN,CHO BIN,SUH BYUNG KYU

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 5 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. Lactic Acidosis in a Congenital Bone Marrow Failure Syndrome;Dubai Medical Journal;2021-05-07

2. Thermodynamic analysis of DNA hybridization signatures near mitochondrial DNA deletion breakpoints;iScience;2021-03

3. Pearson Syndrome: A Rare Cause of Failure to Thrive in Infants;Clinical Pediatrics;2019-03-07

4. Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders;Neuropsychiatric Disease and Treatment;2017-10

5. Anemia arregenerativa en el lactante: 2 casos de síndrome de Pearson;Archivos Argentinos de Pediatria;2017-02-01

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