Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

Annals of Neurology

Volumn 45, Issue 2, 1999, Pages 146-153

  Gleeson, Joseph G ^a,c   Minnerath, Sharon R ^d   Fox, Jeremy W ^a,b   Allen, Kristina M ^a   Luo, Robert F ^a   Hong, Susan E ^a   Berg, Michael J ^e   Kuzniecky, Ruben ^f   Reitnauer, Pamela J ^g   Borgatti, Renato ^h   Mira, Alberto Puche ^k   Guerrini, Renzo ⁱ   Holmes, Gregory L ^c   Rooney, Cynthia M ^c   Berkovic, Samuel ^l   Scheffer, Ingrid ^l   Cooper, Edward C ^m   Ricci, Stefano ^j   Cusmai, Raffaella ^j   Crawford, Thomas O ⁿ   Leroy, Robert ^r   Andermann, Eva ^p   Wheless, James W ^o   Dobyns, William B ^d   Ross, M Elizabeth ^d   Walsh, Christopher A ^a,b,q   more..

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d UNIVERSITY OF MINNESOTA   (United States)

^e UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^f UAB Department of Neurology   (United States)

^g UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^h Scientific Research Institute Eugenio Medea   (Italy)

ⁱ DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

^j BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^k HOSPITAL UNIVERSITARIO VIRGEN DE LA ARRIXACA   (Spain)

^l UNIVERSITY OF MELBOURNE   (Australia)

^m UNIVERSITY OF CALIFORNIA   (United States)

ⁿ JOHNS HOPKINS HOSPITAL   (United States)

^o UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^p MCGILL UNIVERSITY   (Canada)

^q HARVARD INSTITUTES OF MEDICINE   (United States)

^r NONE

more..

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; AMINO ACID SUBSTITUTION; ARTICLE; BRAIN CORTEX; BRAIN MALFORMATION; FEMALE; GENE MUTATION; HETEROTOPIA; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; OPEN READING FRAME; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME LINKED DISORDER;

BRAIN DISEASES; CEREBRAL CORTEX; DNA; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; PEDIGREE; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SYNDROME; X CHROMOSOME;

EID: 0032965786     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(199902)45:2<146::AID-ANA3>3.0.CO;2-N     Document Type: Article

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