Chau Minh Nguyen

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 4

Top Topics

Replacement Therapy

Transcription Factor

Intellectual Disability

Top Venues

BMJ case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Binh Thanh Le, Minh Cuong Duong, Tien Quoc Nguyen, Chau Minh Nguyen
Two siblings with non-classic P450scc deficiency resulted from a novel mutation in CYP11A1 gene misdiagnosed as familial glucocorticoid deficiency. BMJ case reports 15 (12) (2022)
Binh Thanh Le, Minh Cuong Duong, Tien Quoc Nguyen, Chau Minh Nguyen
Two siblings with non-classic P450scc deficiency resulted from a novel mutation in CYP11A1 gene misdiagnosed as familial glucocorticoid deficiency. BMJ case reports 15 (12) (2022)
Binh Thanh Le, Minh Cuong Duong, Tien Quoc Nguyen, Chau Minh Nguyen
Two siblings with non-classic P450scc deficiency resulted from a novel mutation in CYP11A1 gene misdiagnosed as familial glucocorticoid deficiency. BMJ case reports 15 (12) (2022)
Binh Thanh Le, Minh Cuong Duong, Tien Quoc Nguyen, Chau Minh Nguyen
Two siblings with non-classic P450scc deficiency resulted from a novel mutation in CYP11A1 gene misdiagnosed as familial glucocorticoid deficiency. BMJ case reports 15 (12) (2022)