Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency

dbGaP Study Accession: phs000776.v1.p1

Study
phs000776.v1.p1

Variable Name and Accession: Variable Name: SUBJECT_ID
Variable Accession: phv00202352.v1.p1
Variable belongs to dataset: pht003949.v1.p1 : MCCD_Subject_Phenotypes: This subject phenotype table includes subject gender.
Variable Description: De-identified Subject ID
Statistical Summary