Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: Report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively

Journal of Clinical Endocrinology and Metabolism

Volumn 82, Issue 9, 1997, Pages 3063-3067

  Nicolino, Marc ^a   Ferlin, Thérèse ^a   Forest, Maguelone ^a   Godinot, Catherine ^c   Carrier, Henri ^b   David, Michel ^a   Chatelain, Pierre ^a   Mousson, Bénédicte ^a  

^a HÔPITAL DEBROUSSE   (France)

^b INSERM   (France)

^c CENTRE DE GÉNÉTIQUE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADRENAL INSUFFICIENCY; ARTICLE; CASE REPORT; DIABETES MELLITUS; FEMALE; GENE MUTATION; GROWTH RETARDATION; HUMAN; HUMAN TISSUE; KETOACIDOSIS; LEUKODYSTROPHY; MITOCHONDRION; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

ADOLESCENT; ADRENAL INSUFFICIENCY; BASE SEQUENCE; DEAFNESS; DIABETES MELLITUS; DNA, MITOCHONDRIAL; ENDOCRINE SYSTEM DISEASES; FEMALE; GENE DELETION; HISTOCYTOCHEMISTRY; HUMANS; POLYMERASE CHAIN REACTION;

EID: 0030930127     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.82.9.3063     Document Type: Article

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