Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Grewal, Alam S."'
Publikováno v:
Case Reports in Neurology
Mutations in the myelin protein zero (MPZ) gene can cause a variety of clinical and electrophysiological forms of genetic neuropathies including Charcot-Marie-Tooth (CMT) type 1B disease which is characterized by demyelinating features. We present a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fbc00018b505ffe7b4aaaae39b8c21b7
http://europepmc.org/articles/PMC7443678
http://europepmc.org/articles/PMC7443678
Autor:
Oberoi, Kinsi1 (AUTHOR), Grewal, Alam S.2,3 (AUTHOR), Peddareddygari, Leema Reddy2,4 (AUTHOR) lreddy@dynamicbiologics.com
Publikováno v:
Case Reports in Neurology. Jul2020, p255-259. 1 Chart.