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Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
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Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers

Verdonschot, Job A. J. ; Robinson, Emma L. ; James, Kiely N. ; Mohamed, Mohamed W. ; Claes, Godelieve R. F. ; Casas, Kari ; Vanhoutte, Els K. ; Hazebroek, Mark R. ; Kringlen, Gabriel ; Pasierb, Michele M. ; Wijngaard, Arthur ; Glatz, Jan F. C. ; Heymans, Stephane R. B. ; Krapels, Ingrid P. C. ; Nahas, Shareef ; Brunner, Han G. ; Szklarczyk, Radek

Molecular genetics & genomic medicine, 2020-02, Vol.8 (2), p.e1049-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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2
Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction
Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction
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Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction

Greiner, Alexander M ; Freese, Margaret ; Kringlen, Gabriel ; Powers, Edward M ; Gutmann, Rebecca A ; London, Barry

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1) [Periódico revisado por pares]

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3
The Impact of Family History on the Clinical Features of Huntington’s Disease (P4.042)
The Impact of Family History on the Clinical Features of Huntington’s Disease (P4.042)
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The Impact of Family History on the Clinical Features of Huntington’s Disease (P4.042)

Bega, Danny ; Kringlen, Gabriel ; Kinsley, Lisa ; Aufox, Sharon ; Rouleau, Gerald

Neurology, 2018-04, Vol.90 (15_supplement) [Periódico revisado por pares]

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Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers

Verdonschot, Job AJ ; Robinson, Emma L ; James, Kiely N ; Mohamed, Mohamed W ; Claes, Godelieve RF ; Casas, Kari ; Vanhoutte, Els K ; Hazebroek, Mark R ; Kringlen, Gabriel ; Pasierb, Michele M ; van den Wijngaard, Arthur ; Glatz, Jan FC ; Heymans, Stephane RB ; Krapels, Ingrid PC ; Nahas, Shareef ; Brunner, Han G ; Szklarczyk, Radek

MOLECULAR GENETICS & GENOMIC MEDICINE, 2020-02, Vol.8 (2) [Periódico revisado por pares]

WILEY

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