Molecular and Phenotypic Heterogeneity in Mitochondrial Trifunctional Protein Deficiency Due To b-Subunit Mutations

@inproceedings{Spiekerkoetter2003MolecularAP,
  title={Molecular and Phenotypic Heterogeneity in Mitochondrial Trifunctional Protein Deficiency Due To b-Subunit Mutations},
  author={Ute Spiekerkoetter and Bin Sun and Zaza Khuchua and Michael Jennings Bennett and Arnold W. Strauss},
  year={2003}
}
Ute Spiekerkoetter, Bin Sun, Zaza Khuchua, Michael J. Bennett, and Arnold W. Strauss Department of Pediatrics and Vanderbilt Children’s Hospital, Vanderbilt University School of Medicine, Nashville, Tennessee; Heinrich Heine University Hospital, Department of General Pediatrics, Duesseldorf, Germany; Departments of Pathology and Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 

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