Wolfram syndrome in the Polish population: Novel mutations and genotype-phenotype correlation

Clinical Endocrinology

Volumn 75, Issue 5, 2011, Pages 636-641

  Zmyslowska, A ^a   Borowiec, M ^a   Antosik, K ^a   Szalecki, M ^b,c   Stefanski, A ^d   Iwaniszewska, B ^e   Jedrzejczyk, M ^a   Pietrzak, I ^a   Mlynarski, W ^a  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

^b Department of Endocrinology and Diabetology ^*  (Poland)

^c JAN KOCHANOWSKI UNIVERSITY   (Poland)

^d POMERANIAN MEDICAL UNIVERSITY   (Poland)

^e Department of Pediatrics Endocrinology and Neurology   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 4P; CLINICAL ARTICLE; DIABETES MELLITUS; EXON; FEMALE; GENE; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRON; MALE; NUCLEOTIDE SEQUENCE; ONSET AGE; OPTIC NERVE ATROPHY; POLAND; PRIORITY JOURNAL; RARE DISEASE; RELATIVE; SYMPTOM; WFS1 GENE; WOLFRAM SYNDROME;

EID: 80054717689     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2011.04102.x     Document Type: Article

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