A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathy

H. H. Goebel, S. Seddigh, H. C. Hopf, T. Uemichi, Merrill Benson, V. A. McKusick

Research output: Contribution to journalArticle

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)229-230
Number of pages2
JournalNeuromuscular Disorders
Volume7
Issue number4
DOIs
StatePublished - Jun 1997

Fingerprint

Amyloid Neuropathies
Familial Amyloid Neuropathies
Dominant Genes
Prealbumin
Point Mutation
Histidine
Codon
Leucine
Germany
Mutation

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health
  • Developmental Neuroscience
  • Neurology

Cite this

A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathy. / Goebel, H. H.; Seddigh, S.; Hopf, H. C.; Uemichi, T.; Benson, Merrill; McKusick, V. A.

In: Neuromuscular Disorders, Vol. 7, No. 4, 06.1997, p. 229-230.

Research output: Contribution to journalArticle

Goebel, H. H. ; Seddigh, S. ; Hopf, H. C. ; Uemichi, T. ; Benson, Merrill ; McKusick, V. A. / A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathy. In: Neuromuscular Disorders. 1997 ; Vol. 7, No. 4. pp. 229-230.
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