Associated Papers
Phenotype Spectrum of TRPM3-Associated Disorders.
Jolitz L et al.
Annals of Neurology, 2025
39749750 (PubMed )
Supplement: ANA-97-561-s001.docx
Fibulins in development and heritable disease.
Chu ML et al.
Birth Defects Research. Part C, Embryo Today : Reviews, 2004
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes.
Arrondel C et al.
Journal of the American Society of Nephrology : Jasn, 2002
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