Homozygosity mapping of Portuguese and Japanese forms of ataxia-Oculomotor apraxia to 9p13, and evidence for genetic heterogeneity

American Journal of Human Genetics

Volumn 68, Issue 2, 2001, Pages 501-508

  Do Céu Moreira, Maria ^a,b   Barbot, Clara ^b,c   Tachi, Nobutada ^e   Kozuka, Naoki ^e   Mendonça, Pedro ^b   Barros, José ^d   Coutinho, Paula ^b,f   Sequeiros, Jorge ^b   Koenig, Michel ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^b UNIVERSITY OF PORTO   (Portugal)

^c Hospital Maria Pia   (Poland)

^d HOSPITAL DE SANTO ANTÓNIO   (Portugal)

^e SAPPORO MEDICAL UNIVERSITY   (Japan)

^f Hospital de S Sebastião   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATAXIA; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CHROMOSOME 9P; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL FEATURE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; HYPOALBUMINEMIA; JAPAN; MENTAL DEFICIENCY; OPHTHALMOPLEGIA; PERIPHERAL NEUROPATHY; PORTUGAL; PRIORITY JOURNAL;

ATAXIA;

EID: 0035125621     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318191     Document Type: Article

References (21)

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