SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia

Nature Genetics

Volumn 31, Issue 4, 2002, Pages 347-348

  Patel, Heema ^a   Cross, Harold ^a   Proukakis, Christos ^a   Hershberger, Ruth ^a   Bork, Peer ^a   Ciccarelli, Francesca D ^a   Patton, Michael A ^a   McKusick, Victor A ^a   Crosby, Andrew H ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; SPARTIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 13Q; CHROMOSOME MAP; ENDOSOME; FRAMESHIFT MUTATION; GENE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MICROTUBULE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPG20 GENE; TROYER SYNDROME;

ADENOSINE TRIPHOSPHATASES; ADIPOSE TISSUE; CALCIUM-BINDING PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; EXONS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEINS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 0036699065     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng937     Document Type: Article

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