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A novel ATP8 gene mutation in an infant with tetralogy of Fallot.

Tansel, Turkan

A novel ATP8 gene mutation in an infant with tetralogy of Fallot. [electronic resource] - Cardiology in the young Jun 2014 - 531-3 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

ISSN: 1467-1107

Standard No.: 10.1017/S1047951113000668 doi

Subjects--Topical Terms:
Adenosine Triphosphatases--genetics
DNA, Mitochondrial--genetics
Humans
Infant
Male
Mutation
Phospholipid Transfer Proteins--genetics
Tetralogy of Fallot--genetics

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