Zobrazeno 1 - 2
of 2
pro vyhledávání: '"J. P. Kachan"'
Autor:
T V, Asadchuk, N V, Rumiantseva, I V, Naumchik, S A, Likhachev, I V, Pleshko, L V, Shalkevich, I V, Jevneronok, J P, Kachan
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 116(1)
To analyze the molecular defect, a phenotype of hereditary neuropathy with liability to pressure palsies (HNPP, OMIM 162500), in patients with PMP22 gene mutation caused by 1.5 Mb deletion at 17p11.2. and present the principles of diagnosis and genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e39def5a50fbd08912d5e74181969132
https://pubmed.ncbi.nlm.nih.gov/26977628
https://pubmed.ncbi.nlm.nih.gov/26977628
Autor:
I. V. Pleshko, J. P. Kachan, I. V. Jevneronok, I. V. Naumchik, S. A. Likhachev, L. V. Shalkevich, T. V. Asadchuk, N. V. Rumiantseva
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 116:64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b568c9f051da44d2b422842e5cddc8f
https://doi.org/10.17116/jnevro20161161164-69
https://doi.org/10.17116/jnevro20161161164-69