Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum (Q56232649)
Jump to navigation
Jump to search
No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum |
No description defined |
Statements
Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum (English)
0 references
June 2014
0 references
164A
0 references
1614-7
0 references
6
0 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference