Explore
← New search
Filters:
Federico II University Hospital
✕
Reproducible only
✕
mutation analysis / dna sequencing
✕
clear all
1 matching publication(s)
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
PMID 17033964 · · 2006
L1
75/100