We identified a novel homozygous missense mutation (NM_007068.3: c.106G>A, p.Asp36Asn) in <i>DMC1,</i> which cosegregated with NOA and POI phenotypes in this family.
Another POF patient of African origin showed a homozygous nucleotide change in the tenth of DMC1 gene that led to an alteration of the amino acid composition of the protein (M200V).
Another POF patient of African origin showed a homozygous nucleotide change in the tenth of DMC1 gene that led to an alteration of the amino acid composition of the protein (M200V).