Lmbrd1 expression is essential for the initiation of gastrulation

The rare inborn cblF defect of cobalamin metabolism is caused by mutations in the limb region 1 (LMBR1) domain containing 1 gene (LMBRD1). This defect is characterized by massive accumulation of free cobalamin in lysosomes and loss of mitochondrial succinyl‐CoA synthesis and cytosolic methionine syn...

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Detalles Bibliográficos
Autores principales: Buers, Insa, Pennekamp, Petra, Nitschke, Yvonne, Lowe, Chrishanthi, Skryabin, Boris V., Rutsch, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956942/
https://www.ncbi.nlm.nih.gov/pubmed/27061115
http://dx.doi.org/10.1111/jcmm.12844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956942/
https://www.ncbi.nlm.nih.gov/pubmed/27061115
http://dx.doi.org/10.1111/jcmm.12844

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