Knobloch syndrome: Novel mutations inCOL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin-Reference-Cited by-同舟云学术

Knobloch syndrome: Novel mutations inCOL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin

Published:2004-01 Issue:1 Volume:23 Page:77-84
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Menzel Olivier,Bekkeheien Reidunn C.J.,Reymond Alexandre,Fukai Naomi,Boye Eileen,Kosztolanyi Gyorgy,Aftimos Salim,Deutsch Samuel,Scott Hamish S.,Olsen Bjorn R.,Antonarakis Stylianos E.,Guipponi Michel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference35 articles.

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