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Is there sexual dimorphism for coronary artery disease in homozygous familial hypercholesterolemia? Evidence from a kindred of a 60-year-old woman homozygous for W66G mutation in the LDL-receptor gene

✍ Scribed by D. Gaudet; S. Moorjani; G. Tremblay; P. Perron; C. Gagne´; P.-J. Lupien


Book ID
118325207
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
305 KB
Volume
109
Category
Article
ISSN
0021-9150

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