Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency

Statistics

Page Views

Total 151

File Downloads

13023_2012_Article_482.pdf 152

Recent Activity - Last 12 Months


uO Research has been collecting usage data since January 2013. To the best of our ability, this data excludes entries from search engines. Statistics are available at the item, collection and repository level.