A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder-Reference-Cited by-同舟云学术

A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder

Published:2017-09-25 Issue:11 Volume:140 Page:2806-2813
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Shamseldin Hanan E,Alasmari Ali,Salih Mohammed A,Samman Manar M,Mian Shahid A,Alshidi Tarfa,Ibrahim Niema,Hashem Mais,Faqeih Eissa,Al-Mohanna Futwan,Alkuraya Fowzan S

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/140/11/2806/23032279/awx237.pdf

Reference32 articles.

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4. Discovery of mutations for Mendelian disorders;Hum Genet,2016

5. Calcium elevation in mitochondria is the main Ca2+ requirement for mitochondrial permeability transition pore (mPTP) opening;J Biol Chem,2009

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