Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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Genetic studies of human neuropathic pain conditions: a review.

P2860

Q55240474-D1EDB519-4183-4FE0-A60E-5115150A1FF3

P2860

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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2017 nî lūn-bûn

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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Item

label

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

@en

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

@nl

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

@en

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

@nl

P1476

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype

@en

P2093

Brian Meyer

http://www.w3.org/2001/XMLSchema#string

Hamad Al-Zaidan

http://www.w3.org/2001/XMLSchema#string

Haya Al Dosssari

http://www.w3.org/2001/XMLSchema#string

Haya Al Saud

http://www.w3.org/2001/XMLSchema#string

Moeen Al-Sayed

http://www.w3.org/2001/XMLSchema#string

Mohamed A Al-Muhaizea

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Mohammad Al-Owain

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Nadia Alhashemi

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Nadia Sakati

http://www.w3.org/2001/XMLSchema#string

Ola Khalifa

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P2860

Hereditary sensory and autonomic neuropathies: types II, III, and IV

Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factor

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

Improving the physical realism and structural accuracy of protein models by a two-step atomic-level energy minimization

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

Neurotrophin signal transduction in the nervous system.

Fast and accurate long-read alignment with Burrows-Wheeler transform

Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies.

A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception.

Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene.

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1009-1016

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scholarly article

P356

10.1002/AJMG.A.38120

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English

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http://www.w3.org/2001/XMLSchema#string

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173

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Yousef M Binamer

Tariq Ahmad Masoodi

P577

2017-04-01T00:00:00Z

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P698

28328124

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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P2860

P2860

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698