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, HCCSand NDUFB11.
COX7BCOX7BWe are collecting cases with a phenotype suggestive for Linear skin defects with multiple congenital anomalies syndrome (alias MLS syndrome) negative to mutations in COX7b, HCCSand NDUFB11.