Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>.

Nair, Divya; Li, Dong; Erdogan, Hannah; Yoon, Andrew; Harr, Margaret H; Bergant, Gaber; Peterlin, Borut; Pusenjak, Marusa Skrjanec; Jayakar, Parul; Pfundt, Rolph; Jansen, Sandra; McWalter, Kirsty; Sidhu, Alpa; Saliganan, Sheila; Agolini, Emanuele; Jacob, Arthur; Pasquier, Jennifer; Arash, Rafii; Kahrizi, Kimia; Najmabadi, Hossein; Ropers, Hans-Hilger; Bhoj, Elizabeth J

Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3.

Nair, Divya; Li, Dong; Erdogan, Hannah; Yoon, Andrew; Harr, Margaret H; Bergant, Gaber; Peterlin, Borut; Pusenjak, Marusa Skrjanec; Jayakar, Parul; Pfundt, Rolph; Jansen, Sandra; McWalter, Kirsty; Sidhu, Alpa; Saliganan, Sheila; Agolini, Emanuele; Jacob, Arthur; Pasquier, Jennifer; Arash, Rafii; Kahrizi, Kimia; Najmabadi, Hossein; Ropers, Hans-Hilger; Bhoj, Elizabeth J.

HGG Adv ; 3(4): 100122, 2022 Oct 13.

Article en En | MEDLINE | ID: mdl-35860725

ABSTRACT

ABSTRACT

[This corrects the article DOI 10.1016/j.xhgg.2021.100024.].

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: HGG Adv Año: 2022 Tipo del documento: Article