4.7 Article

Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip

期刊

AMERICAN JOURNAL OF HUMAN GENETICS
卷 84, 期 3, 页码 406-411

出版社

CELL PRESS
DOI: 10.1016/j.ajhg.2009.02.002

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资金

  1. NCRR NIH HHS [UL1 RR024153, UL1-RR024153] Funding Source: Medline
  2. NIDCR NIH HHS [R01 DE016148, K02 DE015291-03, R01 DE014667-03, R01 DE014667-02, R01 DE014667-08, P50 DE016215, K02 DE015291, R21 DE016930, K02 DE015291-04, R01 DE014667-04, R21-DE016930, K02 DE015291-01, R01 DE014667-06, P50-DE016215, R37 DE008559, R01-DE016148, R01 DE014667, R01 DE014667-05, R01 DE014667-07, R01 DE014667-01, K02 DE015291-05, K02 DE015291-02, R37-DE08559, R01 DE/HD012324] Funding Source: Medline
  3. NIEHS NIH HHS [P30ES05605, P30 ES005605] Funding Source: Medline

向作者/读者索取更多资源

Cleft lip with or without cleft palate (CL/P) is a complex trait with evidence that the clinical spectrum includes both microform and subepithelial lip defects. We identified missense and nonsense mutations in the BMP4 gene in 1 of 30 cases of microform clefts, 2 of 87 cases with subepithelial defects in the orbicularis oils muscle (OOM), 5 of 968 cases of overt CL/P, and 0 of 529 controls. These results provide confirmation that microforms and subepithelial OOM defects are part of the spectrum of CL/P and should be considered during clinical evaluation of families with clefts. Furthermore, we suggest a role for BMP4 in wound healing.

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