Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Hereditary Neuropathy With Liability To Pressure Palsy[original query] |
---|
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese. Clinical neurology and neurosurgery 2008 May 110 (5): 466-71. Chen Shyue-Ru, Lin Kon-Ping, Kuo Hung-Chou, Chen Chiung-Mei, Hsieh Sung-Tsang, Lee Ming-Jen, Yang Chih-Chao, Liu Chin-San, Huang Chin-Chang, Lyu Rong-Kuo, Ro Long-S |
High frequency of SH3TC2 mutations in Czech HMSN I patients. Clinical genetics 2011 Oct 80 (4): 334-45. Laššuthová P, Mazanec R, Vondrá?ek P, Sišková D, Haberlová J, Sabová J, Seeman |
Clinical and genetic spectra in a series of Chinese patients with Charcot-Marie-Tooth disease. Clinica chimica acta; international journal of clinical chemistry 2015 Oct . Wang Rui, He Jin, Li Jing-Jin, Ni Wang, Wu Zhi-Ying, Chen Wan-Jin, Wang |
- Page last reviewed:Feb 1, 2024
- Content source: