Rapidly progressive infantile cardiomyopathy with mitochondrial respiratory chain complex V deficiency due to loss of ATPase 6 and 8 protein-Reference-Cited by-同舟云学术

Rapidly progressive infantile cardiomyopathy with mitochondrial respiratory chain complex V deficiency due to loss of ATPase 6 and 8 protein

Published:2016-03 Issue: Volume:207 Page:203-205
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Imai Atsuko,Fujita Shuhei,Kishita Yoshihito,Kohda Masakazu,Tokuzawa Yoshimi,Hirata Tomoko,Mizuno Yosuke,Harashima Hiroko,Nakaya Akihiro,Sakata Yasushi,Takeda Atsuhito^ORCID,Mori Masato,Murayama Kei,Ohtake Akira,Okazaki Yasushi

Funder

Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference6 articles.

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2. Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations;Rubio-Gozalbo;Hum. Mutat.,2000

3. Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes;Ware;J. Med. Genet.,2009

4. A comprehensive genomic analysis reveals the genetic landscape of mitochondrial respiratory chain complex deficiencies;Kohda;PLoS Genet.,2016

5. Intractable secretory diarrhea in a Japanese boy with mitochondrial respiratory chain complex I deficiency;Murayama;Eur. J. Pediatr.,2009

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