Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.

J. Erdmann; S. Hassfeld; H. Kallisch; E. Fleck; V. Regitz-Zagrose

doi:10.1002/1098-1004(200011)16:5<448::AID-HUMU19<3.0.CO;2-D

Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.

J. Erdmann^*, S. Hassfeld, H. Kallisch, E. Fleck, V. Regitz-Zagrose

^*Corresponding author for this work

Institute of Cardiogenetics

Deutsches Herzzentrum Berlin

18 Citations (Scopus)

Original language	English
Journal	Human Mutation
Volume	16
Issue number	5
Pages (from-to)	448
Number of pages	1
ISSN	1059-7794
DOIs	https://doi.org/10.1002/1098-1004(200011)16:5<448::AID-HUMU19<3.0.CO;2-D
Publication status	Published - 11.2000

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

SDG 3 Good Health and Well-being
SDG 5 Gender Equality

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Research Area: Medical Genetics

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10.1002/1098-1004(200011)16:5<448::AID-HUMU19<3.0.CO;2-D

Cite this

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title = "Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.",

author = "J. Erdmann and S. Hassfeld and H. Kallisch and E. Fleck and V. Regitz-Zagrose",

year = "2000",

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AU - Erdmann, J.

AU - Hassfeld, S.

AU - Kallisch, H.

AU - Fleck, E.

AU - Regitz-Zagrose, V.

PY - 2000/11

Y1 - 2000/11

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U2 - 10.1002/1098-1004(200011)16:5<448::AID-HUMU19<3.0.CO;2-D

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SN - 1059-7794

VL - 16

SP - 448

JO - Human Mutation

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ER -

Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.

UN SDGs

Research Areas and Centers

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