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Complementary mutations in seipin gene in a patient with Berardinelli–Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene. Issue 10 (17th September 2009)
Record Type:
Journal Article
Title:
Complementary mutations in seipin gene in a patient with Berardinelli–Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene. Issue 10 (17th September 2009)
Main Title:
Complementary mutations in seipin gene in a patient with Berardinelli–Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene