Novel point mutation of the ABC1 gene in Tangier disease with severe syringomyelia-like phenotype and unique endoneurial sclerosis

S Zuchner, A Sperfeld, CO Hanemann, JM Schroder

Research output: Contribution to journal › Article › peer-review

Original language	English
Number of pages	0
Journal	Journal of the Neurological Sciences
Volume	199
Issue number	0
Publication status	Published - 1 Jan 2002

Cite this

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title = "Novel point mutation of the ABC1 gene in Tangier disease with severe syringomyelia-like phenotype and unique endoneurial sclerosis",

author = "S Zuchner and A Sperfeld and CO Hanemann and JM Schroder",

year = "2002",

month = jan,

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language = "English",

volume = "199",

journal = "Journal of the Neurological Sciences",

issn = "0022-510X",

publisher = "Elsevier B.V.",

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TY - JOUR

T1 - Novel point mutation of the ABC1 gene in Tangier disease with severe syringomyelia-like phenotype and unique endoneurial sclerosis

AU - Zuchner, S

AU - Sperfeld, A

AU - Hanemann, CO

AU - Schroder, JM

PY - 2002/1/1

Y1 - 2002/1/1

M3 - Article

SN - 0022-510X

VL - 199

JO - Journal of the Neurological Sciences

JF - Journal of the Neurological Sciences

IS - 0

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