Spinocerebellar ataxias in Spanish patients: Genetic analysis of familial and sporadic cases

Human Genetics

Volumn 104, Issue 6, 1999, Pages 516-522

  Pujana, Miguel Angel ^a   Corral, Jordi ^a   Gratacòs, Mònica ^a   Combarros, Onofre ^b   Berciano, José ^b   Genís, David ^c   Banchs, Isabel ^a   Estivill, Xavier ^a   Volpini, Víctor ^a   Sanchez A ^d   Calopa, M ⁿ   Rosell, J ^e   Cervera, C ^f   Escudero, D ^g   Molina, M ^h   Guitart, M ⁱ   Gabau, E ⁱ   Gutiérrez, J Arpa ^j   Benitez J ^k   Perez De Colosia, V ^l   Villanueva, P ^m   more..

^a HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

^b HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^c HOSPITAL JOSEP TRUETA   (Spain)

^d HOSPITAL CLÍNIC   (Spain)

^e HOSPITAL SON DURETA   (Spain)

^f HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^g HOSPITAL UNIVERSITARI GERMANS TRIAS I PUJOL   (Spain)

^h HOSPITAL DE BASURTO   (Spain)

ⁱ Department of Pediatrics   (Spain)

^j HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^k Hospital UniversitarioFundación Jiménez Díaz   (Spain)

^l Hospital de Merida   (Spain)

^m Section of Pediatric Hemato Oncology Pediatrics Service   (Spain)

ⁿ NONE

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CAUCASIAN; CEREBELLAR ATAXIA; DEGENERATIVE DISEASE; FRIEDREICH ATAXIA; GEOGRAPHIC DISTRIBUTION; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MEIOSIS; MOLECULAR CLONING; ONSET AGE; PRIORITY JOURNAL; SPINOCEREBELLAR TRACT; TRINUCLEOTIDE REPEAT;

ATAXIA; UNCLASSIFIED ORGANISMS;

EID: 0032777834     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050997     Document Type: Article

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