Ratbi, Ilham ;
Falkenberg, Kim D ;
Sommen, Manou...
Ratbi , I , Falkenberg , K D , Sommen , M , Al-Sheqaih , N , Guaoua , S , Vandeweyer , G , Urquhart , J , Chandler , K E , Williams , S , Roberts , N , El Alloussi , M , Black , G , Ferdinandusse , S , Ramdi , H , Heimler , A , Fryer , A , Lynch , S-A , Cooper , N , Ong , K R , Smith , C E L , Inglehearn , C F , Mighell , A J , Elcock , C , Poulter , J A , Tischkowitz , M , Davies , S J , Sefiani , A , Mironov , A , Newman , W , Waterham , H R & Van Camp , G 2015 , ' Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. ' , American Journal of Human Genetics , vol. 97 , no. 4 , pp. 535-545 . https://doi.org/10.1016/j.ajhg.2015.08.011.
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