List of works by Izabela Moszyńska

A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies

scientific article published on 15 October 2009

Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.

scientific article published on 3 November 2010

The 5' regulatory sequence of the PMP22 in the patients with Charcot-Marie-Tooth disease.

scientific article

Paulina is supported by:

About Paulina

Help