Responses

PDF

SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies
Compose Response

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Author Information
First or given name, e.g. 'Peter'.
Your last, or family, name, e.g. 'MacMoody'.
Your email address, e.g. higgs-boson@gmail.com
Your role and/or occupation, e.g. 'Orthopedic Surgeon'.
Your organization or institution (if applicable), e.g. 'Royal Free Hospital'.
Statement of Competing Interests

PLEASE NOTE:

  • Responses are moderated before posting and publication is at the absolute discretion of BMJ, however they are not peer-reviewed
  • Once published, you will not have the right to remove or edit your response. Removal or editing of responses is at BMJ's absolute discretion
  • If patients could recognise themselves, or anyone else could recognise a patient from your description, please obtain the patient's written consent to publication and send them to the editorial office before submitting your response [Patient consent forms]
  • By submitting this response you are agreeing to our full [Response terms and requirements]

Vertical Tabs

Other responses

Jump to comment:

  • Published on:
    Research on burning feet anomaly of HAN1

    Dear Editor,

    I am a member (at least 5th generation) of a family with HSN1. The original article on my family (Riley, H.A. Syringomylia or Myleodysplasia, J Nervous and Mental Disease, vol 72, no. 1, pp. 1-27, 1930) had not identified it as such, but the Riley article has subsequently been referred to in several neurology texts as an example of HSN, Type I. Any researchers investigating this specific neuropathy (HS...

    Show More
    Conflict of Interest:
    None declared.