Clinical utility gene card for: dilated cardiomyopathy (CMD)

Anna Posafalvi; Johanna C. Herkert; Richard J. Sinke; Maarten P. van den Berg; Jens Mogensen; Jan D. H. Jongbloed; J. Peter van Tintelen

doi:10.1038/ejhg.2012.276

Clinical utility gene card for: dilated cardiomyopathy (CMD)

Anna Posafalvi, Johanna C. Herkert, Richard J. Sinke, Maarten P. van den Berg, Jens Mogensen, Jan D. H. Jongbloed, J. Peter van Tintelen^*

^*Corresponding author voor dit werk

Cardiovasculair Centrum

Onderzoeksoutput › Academic › peer review

32 Citaten (Scopus)

Originele taal-2	English
Aantal pagina's	5
Tijdschrift	European Journal of Human Genetics
Volume	21
Nummer van het tijdschrift	10
DOI's	https://doi.org/10.1038/ejhg.2012.276
Status	Published - okt.-2013

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@article{29caedd1f9e04e66abb9e010ea973f94,

title = "Clinical utility gene card for: dilated cardiomyopathy (CMD)",

keywords = "LAMIN-A/C GENE, RIGHT-VENTRICULAR CARDIOMYOPATHY, HYPERTROPHIC CARDIOMYOPATHY, MUTATIONS, COMPOUND, DELETION, DISEASE",

author = "Anna Posafalvi and Herkert, {Johanna C.} and Sinke, {Richard J.} and {van den Berg}, {Maarten P.} and Jens Mogensen and Jongbloed, {Jan D. H.} and {van Tintelen}, {J. Peter}",

year = "2013",

month = oct,

doi = "10.1038/ejhg.2012.276",

language = "English",

volume = "21",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "10",

}

TY - JOUR

T1 - Clinical utility gene card for

T2 - dilated cardiomyopathy (CMD)

AU - Posafalvi, Anna

AU - Herkert, Johanna C.

AU - Sinke, Richard J.

AU - van den Berg, Maarten P.

AU - Mogensen, Jens

AU - Jongbloed, Jan D. H.

AU - van Tintelen, J. Peter

PY - 2013/10

Y1 - 2013/10

KW - LAMIN-A/C GENE

KW - RIGHT-VENTRICULAR CARDIOMYOPATHY

KW - HYPERTROPHIC CARDIOMYOPATHY

KW - MUTATIONS

KW - COMPOUND

KW - DELETION

KW - DISEASE

U2 - 10.1038/ejhg.2012.276

DO - 10.1038/ejhg.2012.276

M3 - Editorial

C2 - 23249954

SN - 1018-4813

VL - 21

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 10

ER -