Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia (Q72073677)

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23 October 2019

title

Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia (English)

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23 October 2019

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T E Ivaschenko

1

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23 October 2019

V S Baranov

series ordinal

2

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23 October 2019

M Dean

series ordinal

3

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23 October 2019

publication date

1 March 1993

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23 October 2019

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23 October 2019

volume

91

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23 October 2019

issue

1

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23 October 2019

page(s)

63-65

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https://scigraph.springernature.com/pub.10.1007/bf00230224

23 October 2019

exact match

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cites work

Screening for cystic fibrosis mutations in Southern France: Identification of a frameshift mutation and two missense variations

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12 December 2020

Benign missense variations in the cystic fibrosis gene

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12 December 2020

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis.

1 reference

12 December 2020

[The frequency of F508 deletion of the mucoviscidosis gene in patients and in families at high risk in Soviet populations]

1 reference

12 December 2020

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

1 reference

12 December 2020

Helpful hints for the detection of single-stranded conformation polymorphisms

1 reference

12 December 2020

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

1 reference

12 December 2020

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1

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12 December 2020

A mutation in the second nucleotide binding fold of the cystic fibrosis gene.

1 reference

12 December 2020

Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR.

1 reference

12 December 2020

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

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12 December 2020

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

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12 December 2020

A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death

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12 December 2020

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium

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12 December 2020

Identifiers

DOI

10.1007/BF00230224

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23 October 2019

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