학술논문
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling
Document Type
Article
Author
Holtz, A.M.; VanCoillie, R.; Vansickle, E.A.; Bupp, C.; Carere, D.A.; Withrow, K.; Torti, E.; Juusola, J.; Millan, F.; Person, R.; Guillen Sacoto, M.J.; Si, Y.; Wentzensen, I.M.; Pugh, J.; Vasileiou, G.; Rieger, M.; Reis, A.; Argilli, E.; Sherr, E.H.; Aldinger, K.A.; Dobyns, W.B.; Brunet, T.; Hoefele, J.; Wagner, M.; Haber, B.; Kotzaeridou, U.; Keren, B.; Heron, D.; Mignot, C.; Heide, S.; Courtin, T.; Buratti, J.; Murugasen, S.; Donald, K.A.; O'Heir, E.; Moody, S.; Kim, K.H.; Burton, B.K.; Yoon, G.; Campo, M.D.; Masser-Frye, D.; Kozenko, M.; Parkinson, C.; Sell, S.L.; Gordon, P.L.; Prokop, J.W.; Karaa, A.; Raby, B.A.
Source
In: Genetics in Medicine . (Genetics in Medicine, October 2022, 24(10):2065-2078)
Subject
Language
English
ISSN
15300366
10983600
10983600