Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland

Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457d...
Ausführliche Beschreibung

Gespeichert in:
Autor*in:

Schubert, Stephanie [verfasserIn]

Haas, Cordula

Bartsch, Christine

Mirshekarnejad, Mandana

Kohrs, Sarah

Roettinger, Irene

Grosshennig, Anika

Stuhrmann, Manfred

Scholz, Caroline

Schmidtke, Jörg

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2015transfer abstract

Schlagwörter:

SIDS

Genetic risk factors

Mutation analysis

TSPYL1

Umfang:

4

Übergeordnetes Werk:

Enthalten in: Metamorphic - Xu, Nanqing ELSEVIER, 2022, London

Übergeordnetes Werk:

volume:29 ; year:2015 ; number:1 ; pages:31-34 ; extent:4

Links:

Volltext

DOI / URN:

10.1016/j.mcp.2014.10.006

Katalog-ID:

ELV039826171

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