A case of N-acetyl galactosaminidase deficiency (Schindler disease) associated with autism

Journal of Autism and Developmental Disorders

Volumn 32, Issue 2, 2002, Pages 145-146

  Blanchon, Y C ^a   Gay, C ^a   Gibert, G ^a   Lauras, B ^a  

^a UNIVERSITY HOSPITAL OF SAINT ETIENNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GALACTOSAMINIDASE; N ACETYLGALACTOSAMINIDASE; UNCLASSIFIED DRUG; BETA N ACETYLHEXOSAMINIDASE; COMPLEMENTARY DNA;

ADOLESCENT; AUTISM; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DISEASE ASSOCIATION; ENZYME DEFICIENCY; GENE LOCATION; HUMAN; LETTER; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; SCHINDLER DISEASE; SOCIAL BEHAVIOR; CHILD; CHROMOSOME 13; CHROMOSOME 22; ENZYMOLOGY; GENETICS;

AUTISTIC DISORDER; CHILD; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 22; DNA, COMPLEMENTARY; HEXOSAMINIDASES; HUMANS; MALE;

EID: 0036526970     PISSN: 01623257     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1017499407910     Document Type: Letter

References (6)

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