A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.
1998 ◽
Vol 101
(7)
◽
pp. 1490-1499
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1990 ◽
Vol 265
(23)
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pp. 13758-13766
1991 ◽
Vol 266
(4)
◽
pp. 2290-2296
Keyword(s):
1986 ◽
Vol 261
(29)
◽
pp. 13844-13849
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Keyword(s):
1991 ◽
Vol 266
(4)
◽
pp. 2297-2302
Keyword(s):
1989 ◽
Vol 264
(33)
◽
pp. 19621-19629
Keyword(s):
1994 ◽
Vol 269
(24)
◽
pp. 16810-16820
Keyword(s):