Atypical Progeroid Syndrome Due to Heterozygous Missense LMNA Mutations

    October 2009 in “ ˜The œJournal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolism ”
    Abhimanyu Garg, Lalitha Subramanyam, Anil K. Agarwal … Yanick J. Crow
    Studysummary In this study, researchers identified novel LMNA mutations in patients with atypical progeroid syndrome, revealing clinical features distinct from other similar disorders, but unrelated to mutant prelamin A accumulation.
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    1. Atypical Progeroid Syndrome Due to Heterozygous Missense LMNA Mutations ˜The œJournal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolism · 2009