| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-102 |
Sentence |
denotes |
Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome. |
| T1 |
0-102 |
Sentence |
denotes |
Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome. |
| TextSentencer_T2 |
103-278 |
Sentence |
denotes |
We present the first family from Italy with the Gerstmann-Sträussler-Scheinker syndrome (GSS) and a substitution of leucine for proline at codon 102 of the prion protein gene. |
| T2 |
103-278 |
Sentence |
denotes |
We present the first family from Italy with the Gerstmann-Sträussler-Scheinker syndrome (GSS) and a substitution of leucine for proline at codon 102 of the prion protein gene. |
| TextSentencer_T3 |
279-368 |
Sentence |
denotes |
This mutation is associated with the ataxic form of GSS in a number of reported families. |
| T3 |
279-368 |
Sentence |
denotes |
This mutation is associated with the ataxic form of GSS in a number of reported families. |
| TextSentencer_T4 |
369-492 |
Sentence |
denotes |
The clinical presentation of our family includes amyotrophic changes in some affected family members in addition to ataxia. |
| T4 |
369-492 |
Sentence |
denotes |
The clinical presentation of our family includes amyotrophic changes in some affected family members in addition to ataxia. |