Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 gene

Neurology

Volumn 58, Issue 6, 2002, Pages 916-921

  Moro, F ^a   Carrozzo, R ^b   Veggiotti, P ^c   Tortorella, G ^d   Toniolo, D ^e   Volzone, A ^a   Guerrini, R ^f  

^a UNIVERSITY OF PISA   (Italy)

^b SAN RAFFAELE HOSPITAL   (Italy)

^c C MONDINO NATIONAL NEUROLOGICAL INSTITUTE   (Italy)

^d UNIVERSITY OF MESSINA   (Italy)

^e CNR   (Italy)

^f UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FILAMIN;

ADOLESCENT; ADULT; AGED; AMINO TERMINAL SEQUENCE; ARTICLE; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; FAMILIAL DISEASE; FEMALE; GENE DELETION; GENE MUTATION; HETEROTOPIA; HUMAN; MALE; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PROTEIN FUNCTION; X CHROMOSOME DOMINANT DISORDER;

EID: 0037177085     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.6.916     Document Type: Article

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