Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.

Human mutation

Volumn 29, Issue 8, 2008, Pages E123-E131

  Nallathambi, Jeyabalan ^a   Laissue, Paul ^b   Batista, Frank ^b   Benayoun, Bérénice A ^b   Lesaffre, Corinne ^b   Moumné, Lara ^b   Pandaranayaka, Pj Eswari ^b   Usha, Kim ^b   Krishnaswamy, Sankaran ^b   Sundaresan, Periasamy ^b   Veitia, Reiner A ^b  

^a ARAVIND MEDICAL RESEARCH FOUNDATION   (India)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

FORKHEAD TRANSCRIPTION FACTOR; FOXL2 PROTEIN, HUMAN;

ANIMAL; ARTICLE; BLEPHAROPHIMOSIS; CELL STRAIN COS1; CERCOPITHECUS; CHILD; FEMALE; FRAMESHIFT MUTATION; GENETICS; HUMAN; INFANT; MALE; MUTATION; PHYSIOLOGY; PREMATURE OVARIAN FAILURE; PRESCHOOL CHILD; PROTEIN TERTIARY STRUCTURE;

ANIMALS; BLEPHAROPHIMOSIS; CERCOPITHECUS AETHIOPS; CHILD; CHILD, PRESCHOOL; COS CELLS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; FRAMESHIFT MUTATION; HUMANS; INFANT; MALE; MUTATION; OVARIAN FAILURE, PREMATURE; PROTEIN STRUCTURE, TERTIARY;

EID: 77957253189     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.20809     Document Type: Article

References (0)