(Q319812)

English

abetalipoproteinemia

Human disease

  • familial hypobetalipoproteinemia
  • microsomal triglyceride transfer protein deficiency disease
  • Bassen-Kornzweig Syndrome
  • Microsomal Triglyceride Transfer Protein Deficiency
  • Bassen-Kornzweig disease
  • Homozygous familial hypobetalipoproteinemia
  • Mtp Deficiency
  • ABETALIPOPROTEINEMIA
  • ABL
  • ABETALIPOPROTEINEMIA; ABL
  • Acanthocytosis
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Abetalipoproteinemia
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Identifiers

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14175366-n
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