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PMID: 10782933
Frossard PM, Dawson KP, Das SJ, Alexander PC, Girodon E, Goossens M
Identification of cystic fibrosis mutations in Oman.
Clin Genet. 2000 Mar;57(3):235-6.,
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
23
ABCC7 p.Ser549Arg
X
ABCC7 p.Ser549Arg 10782933:23:198
status:
NEW
view ABCC7 p.Ser549Arg details
Distribution by ethnicity and by ethnic origins of CF patients and families that were recruited for this study on the population of Oman, and number of alleles carrying either of the two mutations,
S549R
(TG) and DF508 Ethnic origin No. of families No. of patients No. of CF allelesMutation Bedouin descent 1312 22/26S549R(TG) DF508 4/633Baluch origin have other CFTR mutations that have not yet been identified; their sweat chlorides, however, were lower (90-117 mmol/l) and their ages ranged between 3 and 8 years.
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