PMP22 gene-related disorders represent one of the most studied inherited neuropathies due to their genetic clarity and prevalence among hereditary nerve conditions. The evolving understanding of molecular mechanisms is influencing innovation within the Peripheral Myelin Protein 22 (PMP22) Gene-Related Disorder Market.
The most common manifestation, Charcot-Marie-Tooth disease type 1A, results...
Tiếng Việt 
English
Arabic
French
Spanish
Portuguese
Deutsch
Turkish
Dutch
Italiano
Russian
Romaian
Portuguese (Brazil)