A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
about
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityNovel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel.Sustained AAV9-mediated expression of a non-self protein in the CNS of non-human primates after immunomodulation.The Axon-Myelin Unit in Development and Degenerative Disease
P2860
A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
description
2016 nî lūn-bûn
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2016年の論文
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2016年論文
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2016年論文
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2016年論文
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2016年論文
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2016年論文
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2016年论文
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2016年论文
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2016年论文
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name
A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
@en
type
label
A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
@en
prefLabel
A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
@en
P2093
P2860
P1433
P1476
A review of gigaxonin mutations in giant axonal neuropathy (GAN) and cancer.
@en
P2093
Eri S Srivatsan
Isabelle Y Liu
James J Kang
Marilene B Wang
P2860
P2888
P304
P356
10.1007/S00439-016-1659-5
P577
2016-03-29T00:00:00Z
P6179
1034864144