Added by | mollevi |
---|---|
Group name | EquipeLLC |
Item Type | Note |
Note | Lacroix, Matthieu |
Date Added | 2018/11/14 - 11:59:48 |
Date Modified | 2018/11/14 - 11:59:48 |
Parent item | Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutations |