<A> CYP21A2 gene mutation in patients with congenital adrenal hyperplasia. Molecular genetics report from Saudi Arabia

Sarar, Mohamed; Suzan, El Kholy; Nasir, Al Juryyan; Abdulrahman M., Al Nemri; Khaled K., Abu Amero

CYP21A2 gene mutation in patients with congenital adrenal hyperplasia. Molecular genetics report from Saudi Arabia

Sarar, Mohamed; Suzan, El Kholy; Nasir, Al Juryyan; Abdulrahman M., Al Nemri; Khaled K., Abu Amero.

Saudi Medical Journal. 2015; 36 (1): 113-116

in En | IMEMR | ID: emr-159969

Responsible library: EMRO

Subject(s)

Humans; Molecular Biology; Steroid 21-Hydroxylase; Mutation

Search on Google

Add to My VHL

XML

Index: IMEMR Main subject: Steroid 21-Hydroxylase / Molecular Biology / Mutation Limits: Humans Language: En Journal: Saudi Med. J. Year: 2015

Search on Google

Add to My VHL

XML

Index: IMEMR Main subject: Steroid 21-Hydroxylase / Molecular Biology / Mutation Limits: Humans Language: En Journal: Saudi Med. J. Year: 2015