Connection
Catherine Flaitz to Mutation, Missense
This is a "connection" page, showing publications Catherine Flaitz has written about Mutation, Missense.
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0.049 |
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Brown CW, Levy ML, Flaitz CM, Reid BS, Manolidis S, Hebert AA, Bender MM, Heilstedt HA, Plunkett KS, Fang P, Roa BB, Chung P, Tang HY, Richard G, Alford RL. A novel GJB2 (connexin 26) mutation, F142L, in a patient with unusual mucocutaneous findings and deafness. J Invest Dermatol. 2003 Nov; 121(5):1221-3.
Score: 0.049