Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM.

Journal of medical genetics

Volumn 38, Issue 11, 2001, Pages

  Rainier, S ^a   Hedera, P ^a   Alvarado, D ^a   Zhao, X ^a   Kleopa, K A ^a   Heiman Patterson, T ^a   Fink, J K ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE TRIPHOSPHATASE; MICROSATELLITE DNA; SPG3A PROTEIN, HUMAN;

CHILD; CHROMOSOME 14; CHROMOSOME MAP; FAMILY HEALTH; FEMALE; GENETIC LINKAGE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INFANT; LETTER; MALE; PATHOLOGY; PEDIGREE; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 14; FAMILY HEALTH; FEMALE; GTP PHOSPHOHYDROLASES; HUMANS; INFANT; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY;

MLCS; MLOWN;

EID: 0035511840     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.38.11.e39     Document Type: Letter

References (0)