Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -? (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations için istatistikler
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| Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -? (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations | 0 |
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