Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen… - Disease models & …, 2020 - journals.biologists.com
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert, O Olejniczak… - bioRxiv, 2020 - biorxiv.org
The causal genetic underpinnings of congenital heart diseases, which are often complex
and with multigenic background, are still far from understood. Moreover, there are also …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart.

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - europepmc.org
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

[PDF][PDF] Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert, O Olejniczak - 2020 - scholar.archive.org
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen… - Disease models & …, 2020 - pubmed.ncbi.nlm.nih.gov
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - search.proquest.com
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and tetralogy of fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - refubium.fu-berlin.de
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and tetralogy of fallot and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - edoc.mdc-berlin.de
The causal genetic underpinnings of congenital heart diseases, which are often complex
and with multigenic background, are still far from understood. Moreover, there are also …

[HTML][HTML] Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - ncbi.nlm.nih.gov
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and tetralogy of fallot and its functional evaluation in the Drosophila heart

E Auxerre-Plantié, T Nielsen, M Grunert… - Disease Models & …, 2020 - edoc.mdc-berlin.de
The causal genetic underpinnings of congenital heart diseases, which are often complex
and with multigenic background, are still far from understood. Moreover, there are also …