Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the Old Order Mennonites [5]

American Journal of Human Genetics

Volumn 65, Issue 6, 1999, Pages 1785-1790

  Bolk, S ^a   Puffenberger, E G ^a   Hudson, J ^a   Morton, D H ^a   Chakravarti, A ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CONGENITAL NEPHROTIC SYNDROME; CONTROLLED STUDY; FINLAND; GENE AMPLIFICATION; GENE DELETION; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; HAPLOTYPE; HUMAN; INCIDENCE; LETTER; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0033365398     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302687     Document Type: Letter

References (11)

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