TY  - GEN
AU  - Pilz,D T
AU  - Matsumoto,N
AU  - Minnerath,S
AU  - Mills,P
AU  - Gleeson,J G
AU  - Allen,K M
AU  - Walsh,C A
AU  - Barkovich,A J
AU  - Dobyns,W B
AU  - Ledbetter,D H
AU  - Ross,M E
TI  - LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
SN  - 0964-6906
PY  - 1999///0121
KW  - 1-Alkyl-2-acetylglycerophosphocholine Esterase
KW  - Amino Acid Sequence
KW  - Brain
KW  - abnormalities
KW  - DNA
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - Doublecortin Domain Proteins
KW  - Doublecortin Protein
KW  - Exons
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Intellectual Disability
KW  - genetics
KW  - Introns
KW  - Male
KW  - Microtubule-Associated Proteins
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Nervous System Malformations
KW  - Neuropeptides
KW  - Phenotype
KW  - Proteins
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1093/hmg/7.13.2029
ER  -