# doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/doublecortin-a-brain-specific-gene-mutated-in-human-x-linked-lissencephaly-and/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Joseph G. Gleeson,Kristina M. Allen,Jeremy W. Fox,Edward D. Lamperti,Samuel F. Berkovic,Ingrid E. Scheffer,Edward C. Cooper,William B. Dobyns,Sharon Minnerath,M. Elizabeth Ross,Christopher A. Walsh |
| Citations | 1,089 |
| DOI | 10.1016/s0092-8674(00)80899-5 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.cell.com/article/S0092867400808995/pdf |
| OpenAlex ID | https://openalex.org/W2043204105 |
| PMID | 9489700 |
| Type | article |
| Year | 1998 |

## Paper authors

- [Ingrid E. Scheffer](https://scholariq.org/researchers/ingrid-e-scheffer/)

## Paper primary topic

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Paper topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [MicroRNA in disease regulation](https://scholariq.org/topics/microrna-in-disease-regulation/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.