Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology. [electronic resource]
Producer: 20160108Description: 705-11 p. digitalISSN:- 1467-1107
- Cardiomyopathies -- congenital
- Child, Preschool
- DNA, Mitochondrial -- genetics
- Female
- Heart Defects, Congenital -- genetics
- High-Throughput Nucleotide Sequencing -- methods
- Humans
- Infant
- Infant, Newborn
- Male
- Mutation -- genetics
- Polymerase Chain Reaction
- RNA, Ribosomal -- genetics
- RNA, Transfer -- genetics
- Sequence Analysis, DNA -- methods
- Turkey
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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