Familial Lipoprotein Deficiency
العنوان: | Familial Lipoprotein Deficiency |
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المؤلفون: | G. Assmann |
المصدر: | The Lipoprotein Molecule ISBN: 9781468427837 |
بيانات النشر: | Springer US, 1978. |
سنة النشر: | 1978 |
مصطلحات موضوعية: | medicine.medical_specialty, business.industry, Familial high density lipoprotein deficiency, Abetalipoproteinemia, medicine.disease, Hypocholesterolemia, Endocrinology, Tangier disease, Internal medicine, Retinitis pigmentosa, medicine, Familial lipoprotein deficiency, lipids (amino acids, peptides, and proteins), Hypobetalipoproteinemia, business, Lipoprotein |
الوصف: | There are three genetically determined disorders in which one or more of the lipoprotein families are absent from plasma or their concentrations are extremely low: abetalipoproteinemia, hypobetalipoproteinemia, and Tangier disease (familial high density lipoprotein deficiency). Hypocholesterolemia is a common manifestation of all these diseases, which most easily can be distinguished on the basis of clinical symptoms and lipoprotein patterns. |
ردمك: | 978-1-4684-2783-7 |
DOI: | 10.1007/978-1-4684-2781-3_14 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::9f96ea4bcc005955de281fb38ff06cea https://doi.org/10.1007/978-1-4684-2781-3_14 |
رقم الانضمام: | edsair.doi...........9f96ea4bcc005955de281fb38ff06cea |
قاعدة البيانات: | OpenAIRE |
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