Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31 -14.1

European Journal of Human Genetics

Volumn 14, Issue 2, 2006, Pages 249-252

  Bouhouche, Ahmed ^a   Benomar, Ali ^a   Bouslam, Naima ^a   Ouazzani, Reda ^a   Chkili, Taïeb ^a   Yahyaoui, Mohamed ^a  

^a IBN SINA HOSPITAL   (Morocco)

Author keywords

Genetic linkage; Multilating sensory neuropathy; Spastic paraplegia

Indexed keywords

APOLIPOPROTEIN B; CHOLESTEROL; TRIACYLGLYCEROL;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN ELECTROPHYSIOLOGY; CALCULATION; CHILD; CHOLESTEROL BLOOD LEVEL; CHROMOSOME 15P; CHROMOSOME MAP; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; FEMALE; GENETIC LINKAGE; GENETIC RECOMBINATION; GENOME ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; NERVE FIBER; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PRIORITY JOURNAL; RARE DISEASE; SCHOOL CHILD; SCORING SYSTEM; SENSORY DYSFUNCTION; SPINAL CORD COMPRESSION; TRIACYLGLYCEROL BLOOD LEVEL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; GENES, RECESSIVE; HAPLOTYPES; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; LOD SCORE; MALE; MOROCCO; PARAPLEGIA; PEDIGREE;

EID: 31344481370     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201537     Document Type: Article

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