A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V-Reference-Cited by-同舟云学术

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A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V

Published:2001 Issue:4 Volume:49 Page:521-525
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Houlden Henry,King R. H. M.,Hashemi-Nejad A.,Wood N. W.,Mathias C. J.,Reilly Mary,Thomas P. K.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference17 articles.

1. Congenital Insensitivity to Pain with Anhydrosis

2. Anatomic Changes in Congenital Insensitivity to Pain

3. Confirmation of Virtual Unmyelinated Fiber Absence in Hereditary Sensory Neuropathy Type IV

4. NOT ‘INDIFFERENCE TO PAIN’ BUT VARIETIES OF HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY

5. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis

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