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.
NDUFB11
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.