The novel versican p.H2665L homozygous variation is associated with absence of cementum, early teeth loss and recessive Wagner vitreoretinopathy

Bigoni, S (author)

Neri, M (author)

Scotton, C (author)

show more...

Farina, R (author)

Sabatelli, P (author)

Jiang, C (author)

Zhang, J (author)

Falzarano, M (author)

Rossi, R (author)

Ognibene, D (author)

Selvatici, R (author)

Gualandi, F (author)

Bosshardt, D (author)

Perri, P (author)

Campa, C (author)

Brancati, F (author)

Salvatore, M (author)

De Stefano, M (author)

Taruscio, D (author)

Trombelli, L (author)

Fang, M (author)

Ferlini, A (author)

show less...

2019

2019

English.

In: EUROPEAN JOURNAL OF HUMAN GENETICS. - 1018-4813. ; 27, s. 1894-1895

Related links:

http://kipublication...

• Conference paper (other academic/artistic)