-
Abetalipoproteinemia (also
known as: B****en–Kornzweig syndrome,
microsomal triglyceride transfer protein deficiency disease, MTP deficiency, and betalipoprotein...
- selective, as seen in
lactose malabsorption. partial, as
observed in
abetalipoproteinaemia. total, as in
exceptional cases of
coeliac disease.
Routine blood...
-
Lloyd JK,
Wolff OH (1983). "Vitamin E and
Neurological Function:
Abetalipoproteinaemia and
Other Disorders of Fat Absorption". In
Porter R,
Whelan J (eds...
- predominating),
autosomal recessive spinocerebellar ataxia-14 and
abetalipoproteinaemia. An
example of X-linked
ataxic condition is the rare
fragile X-****ociated...
-
disorder that can be
caused by a
mutation in the ApoB gene, APOB.
Abetalipoproteinaemia is
caused by a
mutation in the
microsomal triglyceride transfer...
-
defects in
microsomal triaglyceride transfer protein ****ociated with
abetalipoproteinaemia". Nature. 365 (6441): 65–9. Bibcode:1993Natur.365...65S. doi:10...
-
artery disease and his
recognition in 1960 of the rare
condition of
abetalipoproteinaemia.
Wolff was also co-discoverer of the
Edwards syndrome in abnormal...
-
artery disease and his
recognition in 1960 of the rare
condition of
abetalipoproteinaemia." 1989
David Cornelius Morley "for
transforming the
approach to...
-
defects in
microsomal triglyceride transfer protein ****ociated with
abetalipoproteinaemia". Nature. 365 (6441): 65–9. Bibcode:1993Natur.365...65S. doi:10...
