(Q51576058)
Statements
A G+1 to C mutation in a donor splice site of intron 2 in the apolipoprotein (apo) C-II gene in a patient with apo C-II deficiency. A possible interaction between apo C-II deficiency and apo E4 in a severely hypertriglyceridemic patient. (English)
1 reference
Okubo M
1 reference
Hasegawa Y
1 reference
Aoyama Y
1 reference
Murase T
1 reference
1 April 1997
1 reference
130
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1-2
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153-160
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