Genetic and clinical aspects of lissencephaly;Lissencéphalies: Aspects cliniques et génétiques

Revue Neurologique

Volumn 163, Issue 5, 2007, Pages 533-547

  Verloes, A ^a,b,c   Elmaleh, M ^a,c   Gonzales, M ^d   Laquerriere A ^e   Gressens, P ^a,e  

^a INSERM   (France)

^b HÔpital Necker Enfants Malades   (France)

^c HÔPITAL ROBERT DEBRÉ   (France)

^d ARMAND TROUSSEAU HOSPITAL   (France)

^e ROUEN UNIVERSITY HOSPITAL   (France)

Author keywords

ARX; DCX; Fukuyama; LIS1; Lissencephaly; MEB (Muscle Eye Brain); Microlissencephaly; Miller Dieker; Pahygyria; TUBA3; Walker Warburg

Indexed keywords

DOUBLECORTIN;

AGENESIS; AGYRIA; ARX GENE; CLINICAL FEATURE; CORPUS CALLOSUM; DCX GENE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; GABAERGIC SYSTEM; GASTROESOPHAGEAL REFLUX; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; INCIDENCE; LIS1 GENE; MILLER DIEKER SYNDROME; MUSCLE EYE BRAIN DISEASE; MUSCLE HYPOTONIA; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; REVIEW; TUBA3 GENE; WALKER WARBURG SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 34249873778     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0035-3787(07)90460-9     Document Type: Review

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