LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

Human Molecular Genetics

Volumn 7, Issue 13, 1998, Pages 2029-2037

  Pilz, Daniela T ^a   Matsumoto, Naomichi ^a   Minnerath, Sharon ^b   Mills, Patti ^a   Gleeson, Joseph G ^c,d   Allen, Kristin M ^d   Walsh, Christopher A ^d   Barkovich, A James ^e   Dobyns, William B ^b   Ledbetter, David H ^a   Ross, M Elizabeth ^b  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d HARVARD MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HYDROLASE; MUTANT PROTEIN; PROTEIN;

AGYRIA; ARTICLE; BRAIN MALFORMATION; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 17P; CHROMOSOME XQ; DISEASE SEVERITY; DNA SEQUENCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FRONTAL CORTEX; GENE DELETION; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; OCCIPITAL LOBE; PARIETAL LOBE; POINT MUTATION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 7844223263     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.13.2029     Document Type: Article

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