A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review-Reference-Cited by-同舟云学术

A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review

Author:

Al Shamsi Aisha¹^ORCID,Al Hassani Noura²^ORCID,Hamchou Moustafa³,Almazrouei Raya⁴,Mhanni Aziz⁵

Affiliation:

1. Genetic Division Pediatrics Department Tawam Hospital Al Ain United Arab Emirates

2. Endocrine Division Pediatrics Department Tawam Hospital Al Ain United Arab Emirates

3. Pediatric surgery Division Surgery Department Tawam Hospital Al Ain United Arab Emirates

4. Endocrine Division Internal Medicine Department Tawam Hospital Al Ain United Arab Emirates

5. Department of Pediatrics & Child Health Max Rady College of Medicine Rady Faculty of Health Sciences University of Manitoba Winnipeg Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

Reference14 articles.

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