Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Härönen, H. (H.)"'
Autor:
Kemppainen, A. V. (A. V.), Finnilä, M. A. (M. A.), Heikkinen, A. (A.), Härönen, H. (H.), Izzi, V. (V.), Kauppinen, S. (S.), Saarakkala, S. (S.), Pihlajaniemi, T. (T.), Koivunen, J. (J.)
Mutations in the COL13A1 gene result in congenital myasthenic syndrome type 19 (CMS19), a disease of neuromuscular synapses and including various skeletal manifestations, particularly facial dysmorphisms. The phenotypic consequences in Col13a1 null m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::5d6ebc49adf877fe06248504d428d6f6
http://urn.fi/urn:nbn:fi-fe2022102563245
http://urn.fi/urn:nbn:fi-fe2022102563245
