Alpha-mannosidosis in tunisian consanguineous families: potential involvement of variants in ghr and slc19a3 genes in the variable expressivity of cognitive impairment

HIGHLIGHTS

• who: Rahma Mkaouar and colleagues from the Editor: Azaiez, University of Iowa, UNITED, Children's Hospital Bechir, College of France, Paris, France have published the article: Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment, in the Journal: PLOS ONE of 29/01/2021
• what: The authors report here the clinical and genetic study of six patients from two Tunisian families with AM. This study was approved by the Pasteur Institute in Tunis Review Board (Reference Number:2017/34/E/HRT) and . . .
  

   

  

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