Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

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http://www.wikidata.org/entity/Q51574823
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolateA short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis.Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.Variations in COMT and NTRK2 Influence Symptom Burden in Women Undergoing Breast Cancer Treatment.Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis.Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review.A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis.Genetic studies of human neuropathic pain conditions: a review.
P2860

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Item
http://www.wikidata.org/entity/Q51574823
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2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年學術文章
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name
Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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type
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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Novel NTRK1 mutations cause he ...... ion in the Turkish population.
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P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921