Minigene Analysis of the c.743 + 40A > G Intronic Variant in the <i>CFTR</i> Gene

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ISSN Print: 1949-4998
ISSN Online: 1949-5005
www.scirp.org/journal/health
E-mail: health@scirp.org

"Minigene Analysis of the c.743 + 40A > G Intronic Variant in the CFTR Gene"
written by Ayman El-Seedy, Raed Farhat, Marie-Claude Pasquet, Alain Kitzis, Véronique Ladeveze,
published by Health, Vol.6 No.12, 2014

has been cited by the following article(s):

[1]	N1303K (c. 3909C> G) Mutation and Splicing: Implication of Its c.[744-33GATT (6); 869+ 11C> T] Complex Allele in CFTR Exon 7 Aberrant Splicing
	BioMed Research International, 2015

[2]	N1303K (c. 3909C> G) Mutation and Splicing: Implication of Its c.[744-33GATT (6); 869
	BioMed Research International, 2015

[3]	Acute Intermittent Porphyria in Argentina: An Update
	Human Genetic Diseases, 2015

[4]	Multi-physiopathological consequences of the c. 1392G> T CFTR mutation revealed by clinical and cellular investigations
	Biochemistry and Cell Biology, 2014

[1]	Multi-physiopathological consequences of the c.1392G>T CFTR mutation revealed by clinical and cellular investigations Biochemistry and Cell Biology, 2015 DOI:10.1139/bcb-2014-0042

[2]	N1303K (c.3909C>G) Mutation and Splicing: Implication of Its c.[744-33GATT(6); 869+11C>T] Complex Allele inCFTRExon 7 Aberrant Splicing BioMed Research International, 2015 DOI:10.1155/2015/138103

[3]	Multi-physiopathological consequences of the c.1392G>T CFTR mutation revealed by clinical and cellular investigations Biochemistry and Cell Biology, 2014 DOI:10.1139/bcb-test

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