A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction - Concepedia

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A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction

DOI Full Paper Access

19

Citations

24

References

2011

Year

Ellen H. Jeninga, Monique De Vroede, Nicole Hamers, Johannes M. P. J. Breur, Nanda M. Verhoeven‐Duif, Ruud Berger, Eric Kalkhoven

References

	Year	Citations

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