A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease.
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Genetics ignite focus on microglial inflammation in Alzheimer's diseaseNovel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like familyThe TREM2-DAP12 signaling pathway in Nasu-Hakola disease: a molecular genetics perspective.Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: lesion staging and dynamic changes of axons and microglial subsets.Unique features of mutations revealed by sequentially reprogrammed induced pluripotent stem cells.
P2860
A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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name
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@en
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@nl
type
label
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@en
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@nl
prefLabel
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@en
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@nl
P2093
P1476
A novel compound heterozygous ...... ient with Nasu-Hakola disease.
@en
P2093
Junichi Satoh
Kinya Yamazaki
Kouichi Mizoguchi
Ryo Kuroda
Takashi Yamamura
Tatsuhiro Terada
Tomokazu Obi
Toshiharu Anezaki
P356
10.1016/J.JNS.2006.09.019
P577
2006-11-27T00:00:00Z