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Progeria caused by a rare LMNA mutation p.S143F associated with mild myopathy and atrial fibrillation

Document Type

Article

Author

Madej-Pilarczyk, A.; Fidziańska, A.; Niebrój-Dobosz, I.; Nestorowicz, K.; Hausmanowa-Petrusewicz, I.; Kmieć, T.; Jóźwiak, S.; Rekawek, J.; Turska-Kmieć, A.

Source

In: European Journal of Paediatric Neurology. (European Journal of Paediatric Neurology, September 2008, 12(5):427-430)

Subject

Language

English

ISSN

10903798
15322130

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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