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1750-1172-7-90
1750-1172-7-90
http://dx.doi.org/10.1186/1750-1172-7-90
Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency.
P356
Q42919362-3D1A2676-D600-4A40-9A19-4A7ABEDF1535
P356
1750-1172-7-90
http://dx.doi.org/10.1186/1750-1172-7-90