Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation [2]

American Journal of Human Genetics

Volumn 58, Issue 3, 1996, Pages 636-638

  De Coo, I F M ^a   Smeets, H J M ^a   Gabreels, F J M ^a   Arts, N ^a   Van Oost, B A ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ATAXIA; DNA DETERMINATION; ENZYME ANALYSIS; GENE FREQUENCY; HUMAN; HUMAN CELL; LETTER; MENTAL DEFICIENCY; MITOCHONDRIAL MEMBRANE; PERINATAL ASPHYXIA; POINT MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ATAXIA; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MENTAL RETARDATION; MUSCLES; POINT MUTATION;

ATAXIA;

EID: 0030028562     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)