Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a
Matn3
V194D mutation
2010 ◽
Vol 15
(6)
◽
pp. 835-849
◽
1996 ◽
Vol 63
(1)
◽
pp. 55-61
◽
2010 ◽
Vol 155
(1)
◽
pp. 154-163
◽
2001 ◽
Vol 106
(4)
◽
pp. 244-250
◽
2017 ◽
Vol 14
(4)
◽
pp. 515-519
◽
1976 ◽
Vol 58
(5)
◽
pp. 703-704
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