Associated Papers
Identification of novel RIPK4 variants in a Chinese patient with Arthrogryposis Multiplex Congenita (AMC).
Lu YL et al.
Italian Journal of Pediatrics, 2025
Mental retardation, short stature and synpolydactyly in a manifesting heterozygote of Bartsocas-Papas syndrome.
Abdalla EM et al.
Clinical Genetics, 2013
Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome.
Kalay E et al.
American Journal of Human Genetics, 2012
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