LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification but their existence has not
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LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification but their existence has notThis gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf Hirschhorn syndrome a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8 15 and 19.
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