Search

Your search keyword '"Ohba C"' showing total 4 results

Search Constraints

Start Over You searched for: Author "Ohba C" Remove constraint Author: "Ohba C" Topic genetic predisposition to disease Remove constraint Topic: genetic predisposition to disease
4 results on '"Ohba C"'

Search Results

1. Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing.

2. Genetic analysis of adult leukoencephalopathy patients using a custom-designed gene panel.

3. GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.

4. Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 gene.

Catalog

Books, media, physical & digital resources