Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C &rarr; T mutation

A. Augarten; Y. Yahav; A. Szeinberg; S. Noiman; E. Gazit; B. S. Kerem; Y. Rivlin; A. Tal; H. Blau; L. Ben-Tur; E. Kerem

doi:10.1016/0140-6736(93)91885-P

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation

A. Augarten
, Y. Yahav
, A. Szeinberg
, S. Noiman
, E. Gazit^*
, B. S. Kerem
, Y. Rivlin
, A. Tal
, H. Blau
, L. Ben-Tur
, E. Kerem

^*Corresponding author for this work

Department of Genetics

Research output: Contribution to journal › Article › peer-review

133 Scopus citations

Original language	English
Pages (from-to)	25-26
Number of pages	2
Journal	The Lancet
Volume	342
Issue number	8862
DOIs	https://doi.org/10.1016/0140-6736(93)91885-P
State	Published - 3 Jul 1993

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/0140-6736(93)91885-P

Cite this

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title = "Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C \→ T mutation",

author = "A. Augarten and Y. Yahav and A. Szeinberg and S. Noiman and E. Gazit and Kerem, \{B. S.\} and Y. Rivlin and A. Tal and H. Blau and L. Ben-Tur and E. Kerem",

year = "1993",

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doi = "10.1016/0140-6736(93)91885-P",

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T1 - Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation

AU - Augarten, A.

AU - Yahav, Y.

AU - Szeinberg, A.

AU - Noiman, S.

AU - Gazit, E.

AU - Kerem, B. S.

AU - Rivlin, Y.

AU - Tal, A.

AU - Blau, H.

AU - Ben-Tur, L.

AU - Kerem, E.

PY - 1993/7/3

Y1 - 1993/7/3

UR - https://www.scopus.com/pages/publications/0027278161

U2 - 10.1016/0140-6736(93)91885-P

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C2 - 8100293

AN - SCOPUS:0027278161

SN - 0140-6736

VL - 342

SP - 25

EP - 26

JO - The Lancet

JF - The Lancet

IS - 8862

ER -

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C &rarr; T mutation

UN SDGs

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Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation