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Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660)
Author(s) -
Lanktree M,
Cao H,
Rabkin SW,
Hanna A,
Hegele RA
Publication year - 2007
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2007.00740.x
Subject(s) - lmna , library science , medicine , columbia university , gerontology , genetics , biology , media studies , mutation , sociology , computer science , gene