Novel mitochondrial DNA mutations implicated in Noonan syndrome-Reference-Cited by-同舟云学术

Novel mitochondrial DNA mutations implicated in Noonan syndrome

Published:2007-08 Issue:2 Volume:120 Page:284-285
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Dhandapany Perundurai S.,Sadayappan Sakthivel,Vanniarajan Ayyasamy,Karthikeyan Bose,Nagaraj Chandran,Gowrishankar Kalpana,Selvam Govindan Sadasivam,Singh Lalji,Thangaraj Kumarasamy

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference6 articles.

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2. Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy;Waldmuller;J Mol Cell Cardiol,2003

3. Mitochondrial respiratory-chain diseases;DiMauro;N Engl J Med,2003

4. Clinical and genetic uniqueness in an individual with MELAS;Vanniarajan;Am J Med Genet (Part B),2006

5. Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy;Prasad;Int J Cardiol,2006

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