Coexistence of Amyotrophic Lateral Sclerosis in the Proband of an X-Linked Charcot-Marie-Tooth Disease Type 1 Pedigree in China

참고문헌 (5)

1. Wang Y, "A review of X-linked Charcot-Marie-Tooth disease", J Child Neurol, 31, pp.761~772 (2016)[DOI]
2. Fairweather N, "Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)", Hum Mol Genet, 3, pp.29~34 (1994)[DOI]
3. Brooks BR, "El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis", Amyotroph Lateral Scler Other Motor Neuron Disord, 1, pp.293~299 (2000)[DOI]
4. Sagnelli A, "Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: co-existence of two rare neuromuscular genetic diseases in the same patient", Neuromuscul Disord, 25, pp.800~801 (2015)[DOI]
5. Marchesi C, "Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene", Neuromuscul Disord, 21, pp.129~131 (2011)[DOI]

관련 논문AI추천