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OVOS2 Rabbit Polyclonal Antibody, 50ul Subcellular Fractions Mutations in FMN2 have been

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OVOS2 Rabbit Polyclonal Antibody, 50ul Subcellular Fractions Mutations in FMN2 have been

Store: aashay.com.au · Domain: aashay.com.au

Description

Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47)

ITPKC encodes a member of the inositol 1

Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy)

|Contains 1 PH domain

An important paralog of this gene is TMEM74B

OVOS2 Rabbit Polyclonal Antibody, 50ul Subcellular Fractions Mutations in FMN2 have been

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