LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. [electronic resource]
Producer: 19990121Description: 2029-37 p. digitalISSN:- 0964-6906
- 1-Alkyl-2-acetylglycerophosphocholine Esterase
- Amino Acid Sequence
- Brain -- abnormalities
- DNA -- chemistry
- DNA Mutational Analysis
- Doublecortin Domain Proteins
- Doublecortin Protein
- Exons
- Female
- Genotype
- Humans
- Intellectual Disability -- genetics
- Introns
- Male
- Microtubule-Associated Proteins
- Molecular Sequence Data
- Mutation
- Nervous System Malformations -- genetics
- Neuropeptides -- genetics
- Phenotype
- Proteins -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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