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Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: A mitochondrial DNA depletion disorder

✍ Scribed by Linda M. Randolph; Hollie A. Jackson; Jing Wang; Hiroyuki Shimada; Pedro A. Sanchez-Lara; Derek A. Wong; Lee-Jun Wong; Richard G. Boles


Book ID
116989099
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
378 KB
Volume
102
Category
Article
ISSN
1096-7192

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