Matches in Nanopublications for { ?s ?p "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.
- NP380471.RAet-k0tkY7d4UPEz_mLllVQcX_2Jy9XghJVmo3qrbJ8Y130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380471.RAet-k0tkY7d4UPEz_mLllVQcX_2Jy9XghJVmo3qrbJ8Y130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP839973.RA-THGWQ_JioYjajBoxXcANu7dO6AVTUXRKyAC5rNf35E130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839973.RA-THGWQ_JioYjajBoxXcANu7dO6AVTUXRKyAC5rNf35E130_provenance.
- NP940648.RAaIwoHiWfHgWBMQS6Afo5M1z70_e1q2f8mkUeHGwSj7c130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940648.RAaIwoHiWfHgWBMQS6Afo5M1z70_e1q2f8mkUeHGwSj7c130_provenance.
- assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.