Complementary mutations in seipin gene in a patient with Berardinelli-Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene.

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Author information

Author/s: Wu, Y-R (YR); Hung, S-I (SI); Chang, Y-C (YC); Chen, S-T (ST); Lin, Y-L (YL); Chung, W-H (WH);

Journal and publication information

Publication Type: Case Reports; Letter

Journal: Journal of neurology, neurosurgery, and psychiatry (J Neurol Neurosurg Psychiatry), published in England. (Language: eng)

Reference: 2009-Oct; vol 80 (issue 10) : pp 1180-1

Dates: Created 2009/09/18; Completed 2009/10/08;

PMID: 19762912, status: MEDLINE (last retrieval date: 10/8/2009, IMS Date: )

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