Sort   by:  
 Page size 
UnknownAllele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy.
Not available
S-EPMC5801507 | biostudies-literature
UnknownCongenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Not available
S-EPMC4105259 | biostudies-literature
UnknownPIK3R1 mutations cause syndromic insulin resistance with lipoatrophy.
Not available
S-EPMC3710759 | biostudies-literature
UnknownGenetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome.
Not available
S-EPMC4849793 | biostudies-literature
UnknownMutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.
Not available
S-EPMC3374402 | biostudies-literature
UnknownGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Not available
S-EPMC4835977 | biostudies-literature
Sort   by:  
 Page size