Hereditary myelopathies

CONTINUUM Lifelong Learning in Neurology

Volumn 14, Issue 3, 2008, Pages 58-70

  Fink, John K ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 67650425712     PISSN: 10802371     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.CON.0000324124.55065.09     Document Type: Article

References (13)

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3. Fink JK. The hereditary spastic paraplegias. In: Rosenberg RN, DiMauro S, Paulson HL, et al, editors. The molecular and genetic basis of neurologic and psychiatric disease. 4th ed. Philadelphia: Lippincott Williams & Wilkins, 2007b.
4. Garbern JY, Yool DA, Moore GJ, et al. Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain 2002;125(pt 3):551-561.
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