Primary adrenal insufficiency in a child with a mitochondrial DNA deletion

Journal of Inherited Metabolic Disease

Volumn 21, Issue 2, 1998, Pages 155-161

  Bruno, C ^a   Minetti, C ^b   Tang, Y ^a   Magalhaes P J ^a   Santorelli, F M ^a   Shanske, S ^a   Bado, M ^b   Cordone, G ^b   Gatti, R ^c   DiMauro, S ^a,d  

^a New York Presbyterian Columbia University Medical Center   (United States)

^b UNIVERSITY OF GENOA   (Italy)

^c G GASLINI INSTITUTE   (Italy)

^d Department of Orthopaedic Surgery   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADRENAL INSUFFICIENCY; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; FATALITY; FEMALE; HUMAN; MOLECULAR GENETICS; PRESCHOOL CHILD; RESPIRATORY CHAIN;

ADRENAL INSUFFICIENCY; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; GENE DELETION; HUMANS;

EID: 6844258202     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005347826664     Document Type: Article

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