지원사업
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
- 2020.1
- 수록면
- 347 - 348 (2page)
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참고문헌 (6)
참고문헌 신청
Reid E / 2002 / A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10) / Am J Hum Genet 71:1189~1194
Crimella C / 2012 / Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2 / Clin Genet 82:157~164
Jerath NU / 2015 / Progressive lower extremity weakness and axonal sensorimotor polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln) / Case Rep Genet 2015:496053
Liu YT / 2014 / Extended phenotypic spectrum of KIF5A mutations : from spastic paraplegia to axonal neuropathy / Neurology 83:612~619
Goizet C / 2009 / Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10 / Hum Mutat 30:E376~E385
Crimella C / 2012 / Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2 / Clin Genet 82:157~164
Jerath NU / 2015 / Progressive lower extremity weakness and axonal sensorimotor polyneuropathy from a Mutation in KIF5A (c.611G>A;p.Arg204Gln) / Case Rep Genet 2015:496053
Liu YT / 2014 / Extended phenotypic spectrum of KIF5A mutations : from spastic paraplegia to axonal neuropathy / Neurology 83:612~619
Goizet C / 2009 / Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10 / Hum Mutat 30:E376~E385
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