Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model

Transcription factors SOHLH1 and SOHLH2 coordinate oocyte differentiation without affecting meiosis I

(2017) Yong-Hyun Shin et al.   JOURNAL OF CLINICAL INVESTIGATION

Anticancer sulfonamides target splicing by inducing RBM39 degradation via recruitment to DCAF15

(2017) Ting Han et al.   SCIENCE

Exome sequencing revealed a novel biallelic deletion in theDCAF17gene underlying Woodhouse Sakati syndrome

(2016) R.H. Ali et al.   CLINICAL GENETICS

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure

(2015) S. Katari et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

CRL4–DCAF1 ubiquitin E3 ligase directs protein phosphatase 2A degradation to control oocyte meiotic maturation

(2015) Chao Yu et al.   Nature Communications

Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature

(2014) M. Agopiantz et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

CRL4 Complex Regulates Mammalian Oocyte Survival and Reprogramming by Activation of TET Proteins

(2013) C. Yu et al.   SCIENCE

An investigation of excess residual cytoplasm in human spermatozoa and its distinction from the cytoplasmic droplet

(2012) Anil K Rengan et al.   Reproductive Biology and Endocrinology

The Molecular Basis of CRL4DDB2/CSA Ubiquitin Ligase Architecture, Targeting, and Activation

(2011) Eric S. Fischer et al.   CELL

A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome

(2010) K Steindl et al.   CLINICAL GENETICS

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients

(2010) AM Alazami et al.   CLINICAL GENETICS

Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

(2008) Anas M. Alazami et al.   AMERICAN JOURNAL OF HUMAN GENETICS