Population
Unrelated individuals with familial hypobetalipoproteinaemia
Design
Case_series
Authors
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Hypothesis-generating for apo-B domain roles in hypobetalipoproteinemia; does not support practice changes without larger studies.
The identification of specific apo-B gene mutations causing truncated variants provides insight into domains important for the assembly, secretion, or stability of apo-B-containing lipoproteins in familial hypobetalipoproteinaemia.
Collins et al. (1988) studied this question.
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