Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome (multiple letters)

Human Mutation

Volumn 12, Issue 6, 1998, Pages 431-

  Vincent, J B ^a   Gurling, H M D ^a   Wang, Y C ^a   Li, S Y ^a  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; GENE PRODUCT; UNCLASSIFIED DRUG;

AUTISM; FRAGILE X SYNDROME; HUMAN; INTRON; LETTER; MENTAL DEFICIENCY; POINT MUTATION; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

EID: 0031789982     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1998)12:6<431::AID-HUMU10>3.0.CO;2-Y     Document Type: Letter

References (0)