The spastic paraplegia SPG10 locus: Narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate [7]

Journal of Medical Genetics

Volumn 38, Issue 1, 2001, Pages 65-67

  Reid, E ^a   Escayg, A ^a   Dearlove, A M ^a   Lee, D D ^a   Meisler, M H ^a   Rubinsztein, D C ^a  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN SCN8A; SODIUM ION; UNCLASSIFIED DRUG;

CHROMOSOME 12Q; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 19Q; CHROMOSOME 2P; CHROMOSOME 8Q; CLINICAL FEATURE; GENE LOCUS; GENOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; PRIORITY JOURNAL; SODIUM TRANSPORT; SPASTIC PARAPLEGIA;

EID: 0035133305     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.38.1.65     Document Type: Letter

References (22)

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5. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q
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7. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14p
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