(Q55999492)
English
lissencephaly type 1 due to doublecortin gene mutation
human disease
- XLIS
- Lissencephaly and Agenesis of Corpus Callosum
- Double Cortex Syndrome
- X-linked lissencephaly
- LISSENCEPHALY, X-LINKED, 1
- Lissencephaly X-linked
- LISX
- X-linked lissencephaly type 1
- Lissencephaly, X-Linked, type 1
- LISSENCEPHALY, X-LINKED, 1; LISX1
- Subcortical Laminar Heterotopia, X-Linked
- Subcortical Band Heterotopia, X-Linked
- Dc Syndrome
- Subcortical laminar heterotopia, X-linked,
- LISX1
Statements
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