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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2018.1
- 수록면
- 261 - 263 (3page)
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참고문헌 (5)
참고문헌 신청
Wang Y / 2016 / A review of X-linked Charcot-Marie-Tooth disease / J Child Neurol 31:761~772
Fairweather N / 1994 / Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) / Hum Mol Genet 3:29~34
Brooks BR / 2000 / El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis / Amyotroph Lateral Scler Other Motor Neuron Disord 1:293~299
Sagnelli A / 2015 / 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 25:800~801
Marchesi C / 2011 / 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 21:129~131
Fairweather N / 1994 / Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) / Hum Mol Genet 3:29~34
Brooks BR / 2000 / El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis / Amyotroph Lateral Scler Other Motor Neuron Disord 1:293~299
Sagnelli A / 2015 / 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 25:800~801
Marchesi C / 2011 / 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 21:129~131
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