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1 y recapitulate the phenotype associated with abetalipoproteinemia.
2 es the human lipoprotein deficiency syndrome abetalipoproteinemia.
3 ning lipoproteins, but when defective causes abetalipoproteinemia.
4        Mutations in MTP are a major cause of abetalipoproteinemia.
5 -old Turkish male child with severe signs of abetalipoproteinemia.
6 h cause familial hypobetalipoproteinemia and abetalipoproteinemia.
7 ae from familial hypobetalipoproteinemia and abetalipoproteinemia.
8                                Patients with abetalipoproteinemia, a disease caused by defects in the
9  with conditional intestinal deletion of the abetalipoproteinemia (ABL) gene microsomal triglyceride
10                                              Abetalipoproteinemia (ABL) is a rare Mendelian disorder
11 The serum lipoproteins of five patients with abetalipoproteinemia (ABL) were separated by ultracentri
12 me (DS), cholestatic liver disease (CLD) and abetalipoproteinemia (ABL).
13 absence of a functional 97-kDa subunit cause abetalipoproteinemia, an autosomal recessive disease cha
14                                              Abetalipoproteinemia, an inherited human disease charact
15 f AVED, of cholestatic liver disease, and of abetalipoproteinemia are thought to be due to lack of ci
16 e transfer protein large subunit (lMTP), the abetalipoproteinemia gene product, is tightly controlled
17         Knowledge of the molecular basis for abetalipoproteinemia has led to the development of thera
18 Characterization of mutations in MTP causing abetalipoproteinemia has revealed that the central alpha
19                                              Abetalipoproteinemia is a rare autosomal recessive disor
20 s studies showing that the proximal cause of abetalipoproteinemia is an absence of MTP indicate that
21                                              Abetalipoproteinemia patients with deleterious mutations
22                                  Whether the abetalipoproteinemia previously described and noted in t
23 responsible for the human recessive disorder abetalipoproteinemia, would recapitulate the lipoprotein