HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain.

AuthorsGerald Pfeffer, Helen Griffin, Angela Pyle, Rita Horvath, Patrick F Chinnery
JournalBrain : a journal of neurology (Brain) Vol. 137 Issue Pt 4 Pg. e271 (Apr 2014) ISSN: 1460-2156 [Electronic] England
PMID24271327 (Publication Type: Letter, Comment)
Chemical References
  • Muscle Proteins
  • Protein Kinases
Topics
  • Female
  • Humans
  • Male
  • Muscle Proteins (genetics)
  • Muscular Diseases (complications, genetics)
  • Mutation (genetics)
  • Protein Kinases (genetics)
  • Respiratory Insufficiency (complications, genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: