₃Marie-Laure Moutard

Summary for 2007 [at-glance overview of Marie-Laure Moutard work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Marie-Laure Moutard. According to available data, in 2007 Marie-Laure Moutard published at least 3 articles. This work was completed in collaboration with several authors including Fryns, Jean-Pierre and Lacombe, Didier. Many other authors have collaborated with Marie-Laure Moutard as well. There is no information about the funding or the grants awarded to support this work.

Marie-Laure Moutard has rank 482 when compared to all other authors using the keyword Phenotype. Analysis of the article abstracts and the titles suggests that Marie-Laure Moutard professional interests are focused around "biallelic prodh mutations", "clinical molecular phenotype" and "phenotype children biallelic". These might also be referred to as "biallelic prodh", "prodh mutations" or "neurological phenotype". Statistical analysis shows that Marie-Laure Moutard's writing is likely to contains terms "mutations", "patients", "prodh", "phenotype", "neurological" and "trex1".

Unfortunately, there is not enough information to establish Marie-Laure Moutard affiliation. Luckily, one email address is on file.

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