[HTML][HTML] A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- The American Journal of�…, 1998 - cell.com
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
[CITATION][C] A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- The American Journal�…, 1998 - cir.nii.ac.jp
A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive
Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at�…
Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at�…
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat�…
MD Lalioti, HS Scott, P Genton…�- …�journal of human�…, 1998 - pubmed.ncbi.nlm.nih.gov
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
[HTML][HTML] A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- The American Journal of�…, 1998 - Elsevier
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- The American Journal of�…, 1998 - infona.pl
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
[PDF][PDF] A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- Am. J. Hum�…, 1998 - academia.edu
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- American journal of�…, 1998 - folia.unifr.ch
English Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
[PDF][PDF] A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of�…
MD Lalioti, HS Scott, P Genton, R Ouazzani…�- Am. J. Hum�…, 1998 - core.ac.uk
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6–16 years, generalized�…
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat�…
MD Lalioti, HS Scott, P Genton…�- American Journal of�…, 1998 - ncbi.nlm.nih.gov
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare,
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
autosomal recessive disorder characterized by onset at age 6-16 years, generalized�…
[CITATION][C] A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of�…
MD LALIOTI, HS SCOTT, A BOTTANI…�- American journal of�…, 1998 - pascal-francis.inist.fr
A PCR amplification method reveals instability of the dodecamer repeat in progressive
myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at�…
myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at�…