Journal Article

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

M. Hergersberg; Jaya Balakrishnan; Thomas Bettecken; Francoise Chevalier-Porst; Christian Brägger; René Burger; Inge Einschenk; Sabina Liechti-Gallati; Michael Morris; Daniel Schorderet; Francine Thonney; Hans Moser; Naseem Malik

Human Genetics · Vol. 100, Issue 2 · pp. 220-223 · 1997

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	1997-07-09
Publication Year	1997
Volume	100
Issue	2
Pages	220-223
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s004390050494

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NARA Access Coverage	1964-01-01~Current
Journal Homepage	https://www.springer.com/journal/439
Publisher Page	Open Publisher Page

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