Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all synonyms
A novel SLC25A32 homozygous variant is associated with severe neuromuscular phenotype.
SLC25A32 gene polymorphism could be a risk factor for lower folate concentration and future fracture.
Compares and contrasts all the known human SLC25A (show SLC25A25 ELISA Kits)* genes and includes functional information.
identified residues in the walls and at the base of the transport cavity that are involved in substrate recognition by the MFT
Patient with SLC25A32 deficiency was able to have a successful pregnancy after fertilization in vitro.
This gene encodes a member of the P(I/L)W subfamily of mitochondrial carrier family transport proteins. The encoded protein transports folate across the inner mitochondrial membrane. Alternatively spliced transcript variants have been described.
mitochondrial folate transporter/carrier
, solute carrier family 25, member 32
, solute carrier family 25 (mitochondrial folate carrier) , member 32