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1471-2350-15-71
1471-2350-15-71
https://scigraph.springernature.com/pub.10.1186/1471-2350-15-71
Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy.
P2888
Q30833220-3AC4FE98-404D-4F9A-B76D-B912EFAE1DFB
P2888
1471-2350-15-71
https://scigraph.springernature.com/pub.10.1186/1471-2350-15-71