Frequency of mutations for glycogen storage disease type II in different populations: The Δ525T and Δexon 18 mutations are not generally 'common' in white populations [1]

Journal of Medical Genetics

Volumn 36, Issue 1, 1999, Pages 85-86

  Hirschhorn, R ^a   Huie, M L ^a  

^a NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN;

ALLELE; CAUCASIAN; CONTROLLED STUDY; EXON; GENE FREQUENCY; GENE MUTATION; GLYCOGEN STORAGE DISEASE TYPE 2; HETEROZYGOSITY; HUMAN; HUMAN CELL; LETTER; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

ALLELES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FOUNDER EFFECT; GENETIC SCREENING; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; MUTATION; NETHERLANDS;

EID: 0032910682     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (9)