Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity

Neuropediatrics

Volumn 29, Issue 4, 1998, Pages 189-194

  Topaloglu H ^a   Pinarli, G ^b   Erdem, H ^a   Gucuyener K ^b   Karaduman, A ^a   Topcu M ^a   Akarsu, A N ^a   Ozguc M ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b GAZI UNIVERSITY FACULTY OF MEDICINE   (Turkey)

Author keywords

Autosomal recessive; Complicated form; Genetic heterogeneity; Hereditary spastic paraplegia; Pure form

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN DISEASE; CHROMOSOME 8P; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; GENE MAPPING; GENETIC HETEROGENEITY; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOTE; HUMAN; HUMAN CELL; HYPERREFLEXIA; MALE; MENTAL DEFICIENCY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SCHOOL CHILD; SPHINCTER;

EID: 0031877966     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973559     Document Type: Article

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