Concepedia

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

Koki Yamada, Caroline Andrews, Wai‐Man Chan, Craig A. McKeown, Adriano Magli, Teresa de Berardinis, Anat Loewenstein, Moshé Lazar, Michael O’Keefe, Robert D. Letson,

Nature Genetics · 2003 · 262 citations · 14 references

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14

Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

Chunjie Zhao, Junko Takita, Yosuke Tanaka et al. · Cell · 2001 · 760 citations · Full text

, , +14

A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

Evan Reid, Mark Kloos, Allison E. Ashley‐Koch et al. · The American Journal of Human Genetics · 2002 · 540 citations · Full text

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Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles

Elizabeth C. Engle, Boyan C. Goumnerov, Craig A. McKeown et al. · Annals of Neurology · 1997 · 175 citations

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Novel Dendritic Kinesin Sorting Identified by Different Process Targeting of Two Related Kinesins: KIF21A and KIF21B

Joseph R. Marszalek, Joshua A. Weiner, Samuel J. Farlow et al. · The Journal of Cell Biology · 1999 · 165 citations · Full text

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CFEOM3: a new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3.

E J Doherty, Margaret E. Macy, S.M. Wang et al. · PubMed · 1999 · 104 citations

, , +15