Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations [3]

Thorax

Volumn 58, Issue 6, 2003, Pages 552-554

  Kispert, A ^a   Petty, M ^a   Olbrich, H ^b   Volz, A ^b   Ketelsen, U P ^b   Horvath, J ^b   Melkaoui, R ^b   Omran, H ^b   Zariwala, M ^c   Noone, P G ^c   Knowles, M ^c  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b UNIVERSITY OF FREIBURG   (Germany)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 19Q; CHROMOSOME 9P; CILIARY DYSKINESIA; DNAH5 GENE; GENE; GENE EXPRESSION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; LETTER; PRIORITY JOURNAL;

GENOTYPE; HUMANS; KARTAGENER SYNDROME; MUTATION; PHENOTYPE;

EID: 0038808827     PISSN: 00406376     EISSN: None     Source Type: Journal    
DOI: 10.1136/thorax.58.6.552     Document Type: Letter

References (11)

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