The association between haematological manifestation and mtDNA deletions in Pearson syndrome

Journal of Inherited Metabolic Disease

Volumn 20, Issue 5, 1997, Pages 697-703

  Muraki, K ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ACIDOSIS; ADOLESCENT; ARTICLE; BLOOD CELL; BONE MARROW CELL; CASE REPORT; CHILD; FEMALE; GENE DELETION; HUMAN; KEARNS SAYRE SYNDROME; MALE; NEUTROPENIA; NEWBORN; PANCYTOPENIA; PEARSON SYNDROME; PRESCHOOL CHILD; REFRACTORY ANEMIA; SOUTHERN BLOTTING; THROMBOCYTOPENIA;

ADOLESCENT; BLOOD CELL COUNT; BONE MARROW DISEASES; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; GENE DELETION; HEMATOLOGIC DISEASES; HUMANS; INFANT, NEWBORN; MALE;

EID: 0030800458     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005378527077     Document Type: Article

References (13)

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