Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation-Reference-Cited by-同舟云学术

Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation

Author:

Rosti R.O.¹,Uyguner Z.O.²,Nazarenko I.³,Bekerecioglu M.⁴,Cadilla C.L.⁵,Ozgur H.²,Lee B.H.³⁶,Aggarwal A.K.⁷,Pehlivan S.⁸,Desnick R.J.³

Affiliation:

1. Department of Neurosciences; University of California; San Diego CA USA

2. Department of Medical Genetics; Istanbul University, Istanbul Medical Faculty; Istanbul Turkey

3. Department of Genetics and Genomic Sciences; Icahn School of Medicine at Mount Sinai; New York NY USA

4. Department of Plastic, Reconstructive and Aesthetic Surgery; Necmettin Erbakan University, Meram Faculty of Medicine; Konya Turkey

5. Department of Biochemistry; University of Puerto Rico School of Medicine; San Juan PR USA

6. Department of Pediatrics, Asan Medical Center; University of Ulsan College of Medicine; Seoul Korea

7. Department of Structural and Chemical Biology; Icahn School of Medicine at Mount Sinai; New York NY USA

8. Department of Medical Biology; Istanbul University, Istanbul Medical Faculty; Istanbul Turkey

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Congenital ectodermal dysplasia of the face;Setleis;Pediatrics,1963

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