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PMID: 1944451 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels.

The New England journal of medicine ·Vol. 325 ·No. 23 ·1991-12-05 ·Pages 1630-4

Strong TV, Smit LS, Turpin SV, Cole JL, Hon CT, Markiewicz D, Petty TL, Craig MW, Rosenow EC, Tsui LC

Abstract

暂无摘要

Related Genes

cftr

MeSH Terms

Base Sequence Cystic Fibrosis/genetics,metabolism DNA/analysis Electrolytes/analysis Exons Female Humans Middle Aged Molecular Sequence Data Mutation Sweat/chemistry

Chemicals

Electrolytes DNA

Authors & Affiliations

10 authors, click to expand affiliations / ORCID

Strong T V

Howard Hughes Medical Institute, Ann Arbor, MI 48109-0650.

Smit L S

Turpin S V

Cole J L

Hon C T

Markiewicz D

Petty T L

Craig M W

Rosenow E C

Tsui L C

Article Info

Journal

The New England journal of medicine

Abbr.

N Engl J Med

ISSN

0028-4793

DOI

10.1056/NEJM199112053252307

Published

1991-12-05

Pages

1630-4

Language

English

Region

United States

NLM ID

0255562

Subset

Grants

NCRR NIH HHS · M01-RR00046 · United States

NIDDK NIH HHS · P01-DK42718 · United States

NIDDK NIH HHS · R01-DK39690 · United States

External Links

PubMed source DOI: 10.1056/NEJM199112053252307 View journal details

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Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels.

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