We are collecting cases with a phenotype suggestive for Linear skin defects with multiple congenital anomalies syndrome (alias MLS syndrome) negative to mutations in COX7b,HCCS and NDUFB11.
NDUFB11NDUFB11We are collecting cases with a phenotype suggestive for Linear skin defects with multiple congenital anomalies syndrome (alias MLS syndrome) negative to mutations in COX7b,HCCS and NDUFB11.