Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient

N. Dharajiya, K. M. Chisholm, L. Dietz, Carolyn (Sue) Richards, M. Kharrazi, I. Schrijver

Research output: Contribution to journalArticle

1 Citation (Scopus)
Original languageEnglish (US)
Pages (from-to)598-599
Number of pages2
JournalClinical Genetics
Volume83
Issue number6
DOIs
StatePublished - Jun 2013

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DNA Mutational Analysis
Poly T
Founder Effect
Cystic Fibrosis Transmembrane Conductance Regulator
Hispanic Americans
Cystic Fibrosis
Alleles
Newborn Infant
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient. / Dharajiya, N.; Chisholm, K. M.; Dietz, L.; Richards, Carolyn (Sue); Kharrazi, M.; Schrijver, I.

In: Clinical Genetics, Vol. 83, No. 6, 06.2013, p. 598-599.

Research output: Contribution to journalArticle

Dharajiya, N. ; Chisholm, K. M. ; Dietz, L. ; Richards, Carolyn (Sue) ; Kharrazi, M. ; Schrijver, I. / Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient. In: Clinical Genetics. 2013 ; Vol. 83, No. 6. pp. 598-599.
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