Concepedia

Prion disease with 144 base pair insertion in a Japanese family line

Tatsuro Oda, Tetsuyuki Kitamoto, Jun Tateishi, Tsukasa Mitsuhashi, K Iwabuchi, Chie Haga, Eiichi Oguni, Yuji Kato, Itaru Tominaga, Kiyoshi Yanai,

Acta Neuropathologica · 1995 · 41 citations · 15 references

DOI

Concepts

References

15

Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome

Karen Hsiao, Harry F. Baker, Tim Crow et al. · Nature · 1989 · 847 citations

, , +14

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

Lev G. Goldfarb, Paul Brown, W. Richard McCombie et al. · Proceedings of the National Academy of Sciences · 1991 · 332 citations · Full text

, , +17

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

Tetsuyuki Kitamoto, R W Shin, Katsumi Doh‐ura et al. · PubMed · 1992 · 270 citations

, , +12

Novel Missense Variants of Prion Protein in Creutzfeldt-Jakob Disease or Gerstmann-Sträussler Syndrome

Tetsuyuki Kitamoto, Mika Ohta, Katsumi Doh‐ura et al. · Biochemical and Biophysical Research Communications · 1993 · 171 citations

, , +17

INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES

John Collinge, Jeremy M. Brown, John Hardy et al. · Brain · 1992 · 171 citations

, , +17