Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy. (Q30833220)
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English | Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy. |
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Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy (English)
Shahid Mahmood Baig
Tahir Naeem Khan
Muhammad Tariq
Pakeeza Arzoo Shaiq
Katrin Mäbert
1 reference
1 reference