其他Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.
期刊:Human molecular genetics发表年份:2008作者:Anna Rajab; Daniel Kelberman; Sandra C P de Castro; Heike Biebermann; Hala Shaikh; Kerra Pearce; Catherine M Hall; Guftar Shaikh; Dianne Gerrelli; Annette Grueters; Heiko Krude; Mehul T Dattani
