A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype.

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Serval ID
serval:BIB_2711
Type
Article: article from journal or magazin.
Collection
Publications
Institution
UNIL/CHUV
Title
A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype.
Journal
Human Genetics
Author(s)
Hergersberg M, Balakrishnan J, Bettecken T, Chevalier-Porst F, Bragger C, Burger R, Einschenk I, Liechti-Gallati S, Morris M, Schorderet D, Thonney F, Moser H, Malik N
Publication state
Published
Issued date
1997
Volume
100
Pages
220-223
OAI-PMH
oai:serval.unil.ch:BIB_2711
Create date
19/11/2007 13:23
Last modification date
20/08/2019 14:05
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