Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence

Journal of Human Genetics

Volumn 45, Issue 3, 2000, Pages 167-170

  Sakamoto, Michiko ^a   Ono, Jiro ^a   Okada, Shintaro ^a   Nakamura, Yusuke ^a,b   Kurahashi, Hiroki ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

DCX gene; Isolated lissencephaly sequence; Subcortical laminar heterotopia

Indexed keywords

AGYRIA; ARTICLE; BRAIN MALFORMATION; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; GENE STRUCTURE; HETEROTOPIA; HUMAN; JAPAN; MALE; POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME LINKED DISORDER;

EID: 0034080899     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380050204     Document Type: Article

References (17)

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