Associated Papers
Complementary mutations in seipin gene in a patient with Berardinelli-Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene.
Wu YR et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2009
A variable neurodegenerative phenotype with polymerase gamma mutation.
Stricker S et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2009
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