Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia

Journal of Medical Genetics

Volumn 43, Issue 5, 2006, Pages 441-443

  Bouhouche, A ^a   Benomar, A ^a   Bouslam, N ^a   Chkili, T ^a   Yahyaoui, M ^a  

^a IBN SINA HOSPITAL   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CHAPERONIN; HISTIDINE;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CCT5 GENE; CONTROLLED STUDY; EXON; FAMILY STUDY; GENE; GENE SEGREGATION; GENE SEQUENCE; HUMAN; MISSENSE MUTATION; PRIORITY JOURNAL; SENSORY NEUROPATHY; SEQUENCE ANALYSIS; SPASTIC PARAPLEGIA;

AMINO ACID SEQUENCE; CHAPERONINS; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MOLECULAR CHAPERONES; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PEDIGREE; PROTEIN SUBUNITS; SEQUENCE ALIGNMENT; SPASTIC PARAPLEGIA, HEREDITARY;

ANIMALIA;

EID: 33646432730     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2005.039230     Document Type: Article

References (21)

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