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|
Appointment Type |
Department |
Division |
Rank |
| Primary |
Genetics |
Clinical Genetics |
Professor |
| Secondary |
Genetics |
Clinical Genetics |
Associate Professor |
| Secondary |
Pediatrics |
Ped - General Pediatrics |
Professor |
|
|
Organization Name |
Position Held |
Org Link |
| American Academy of Pediatrcis |
|
|
| American Society of Human Genetics |
|
|
| Child Neurology Society |
|
|
| Socieity for inherited Metabolic Disorders |
|
|
| The Society for the Study of Inborn Errors of Metabolism |
|
|
|
| Publication |
PUBMEDID |
A new genetic disorder in mitochondrial fatty acid β-oxidation: new insights into fatty acid metabolism. He M., Rutledge SL, Kelly D,Palmer CA, Murdoch. J, Majumder, N , Nicolls RD, Matern D, Vockley J. Am J Hum Genetics, 81: 87-103, 2007.
|
17564966 |
Abnormal white matter in a neurologically intact child with Incontinentia Pigmenti. Bryant SA, Rutledge SL. Pediatric Neurology, 36: 199-202, 2007. |
17352958 |
| Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyl transferase 1 deficiency. MJ Bennett, RL Boriack, S Narayan, SL Rutledge , ML Raff. Molecular Genetics & Metabolism. 82(1):59-63, 2004 May. |
15110323 |
|
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