Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Charcot-Marie-Tooth Disease and HINT1[original query] |
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Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2. Neurogenetics 2019 12 21 (2): 79-86. Lin Shan, Xu Liu-Qing, Xu Guo-Rong, Guo Ling-Ling, Lin Bi-Juan, Chen Wan-Jin, Wang Ning, Lin Yi, He J |
Rare among Rare: Phenotypes of Uncommon CMT Genotypes. Brain sciences 2021 12 11 (12): . Gentile Luca, Russo Massimo, Taioli Federica, Ferrarini Moreno, Aguennouz M'Hammed, Rodolico Carmelo, Toscano Antonio, Fabrizi Gian Maria, Mazzeo An |
HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease. Journal of the peripheral nervous system : JPNS 2021 10 26 (4): 444-448. Kontogeorgiou Zoi, Voudommatis Charalampos, Kartanou Chrisoula, Pandis Dionysis, Breza Marianthi, Zambelis Thomas, Stefanis Leonidas, Panas Marios, Koutsis Georgios, Karadima Georg |
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