Acads gene deletion in BALB/cByJ mouse strain occurred after 1981 and is not present in BALB/cByJ-fld mutant mice

Mammalian Genome

Volumn 7, Issue 9, 1996, Pages 694-695

  Reue, K ^a,b   Cohen, R D ^a,b  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; ACYL COENZYME A DESATURASE; PRIMER DNA;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; ENZYMOLOGY; FATTY LIVER; GENE; GENE DELETION; GENETICS; MOLECULAR GENETICS; MOUSE; MOUSE MUTANT; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION;

ACYL-COA DEHYDROGENASE; ANIMALS; BASE SEQUENCE; DNA PRIMERS; FATTY ACID DESATURASES; FATTY LIVER; GENE DELETION; GENES; MICE; MICE, INBRED BALB C; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION;

EID: 0030239680     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900208     Document Type: Article

References (10)

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2. Amendt, B.A., Freneaux, E., Reece, C., Wood, P.A., Rhead, W.J. (1992). Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouse. Pediatr. Res. 31, 552-556.
3. Coates, P.M., Hale, D.E., Finocchiaro, G., Tanaka, K., Winter, S.M. (1988). Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness. J. Clin. Invest. 81, 171-175.
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