Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis

Human Genetics

Volumn 106, Issue 6, 2000, Pages 594-596

  Hulme, Dennis J ^a,b   Blair, Ian P ^a,b   Dawkins, Jennifer L ^a,b   Nicholson, Garth A ^a,b  

^a NATIONAL INSTITUTE OF HYDROLOGY   (India)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; MESSENGER RNA;

ARTICLE; CHROMOSOME 9Q; GENE MUTATION; HEARING LOSS; HUMAN; HUMAN TISSUE; MOTONEURON; NEUROPATHY; NORTHERN BLOTTING; PATHOGENESIS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SENSORY NERVE CELL;

BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTORS; BLOTTING, NORTHERN; BRAIN; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA-BINDING PROTEINS; G-BOX BINDING FACTORS; GENE EXPRESSION; GENETIC SCREENING; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; LUNG; MOLECULAR SEQUENCE DATA; ORGAN SPECIFICITY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; SPINAL CORD; TRANSCRIPTION FACTORS;

EID: 0033935141     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050030     Document Type: Article

References (7)

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