SCOPUS 정보 검색 플랫폼

Volumn 67, Issue 5, 2000, Pages 1320-1326

Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34

(9) Nemeth, Andrea H a,b Bochukova, Elena a Dunne, Eimear a Huson, Susan M b Elston, John c Hannan, Mohammed A e Jackson, Matthew d Chapman, Cyril J b Taylor, A Malcolm R f

a UNIVERSITY OF OXFORD (United Kingdom)

b CHURCHILL HOSPITAL (United Kingdom)

c OXFORD EYE HOSPITAL (United Kingdom)

d RADCLIFFE INFIRMARY (United Kingdom)

e KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER (Saudi Arabia)

f UNIVERSITY OF BIRMINGHAM (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APRAXIA; ARTICLE; ATAXIA; ATAXIA TELANGIECTASIA; AUTOSOMAL RECESSIVE DISORDER; CEREBELLAR ATAXIA; CHOREOATHETOSIS; CHROMOSOME 3Q; CLINICAL FEATURE; DEGENERATIVE DISEASE; FAMILY STUDY; GENE MAPPING; GENETIC LINKAGE; GENETIC STABILITY; HOMOZYGOSITY; HUMAN; IMMUNE DEFICIENCY; NEOPLASM; OPHTHALMOPLEGIA; PEDIGREE; PRIORITY JOURNAL;

ATAXIA; ATAXIA TELANGIECTASIA;

EID: 0033754489 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1016/S0002-9297(07)62962-0 Document Type: Article

Times cited : (88)

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