Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death

Pediatric Neurology

Volumn 15, Issue 2, 1996, Pages 145-149

  Santorelli, Filippo M ^a   Schlessel, Jerrold S ^b   Slonim, Alfred E ^c   DiMauro, Salvatore ^a,d  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b NORTH SHORE UNIVERSITY HOSPITAL   (United States)

^c Department of Obstetrics Gynecology   (United States)

^d NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCINE; MITOCHONDRIAL DNA; TRANSFER RNA;

ARTICLE; ASTHMA; ATTENTION DEFICIT DISORDER; BRAIN DISEASE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; FEMALE; GASTROESOPHAGEAL REFLUX; GENE MUTATION; HUMAN; INFANT; LEARNING DISORDER; MALE; MEDICAL RECORD; NEUROLOGIC EXAMINATION; PEDIGREE; PRIORITY JOURNAL; SINUSITIS; SUDDEN INFANT DEATH SYNDROME;

EID: 0030249144     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/0887-8994(96)00163-4     Document Type: Article

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