Search

Your search keyword '"MHBD deficiency"' showing total 1 results

Search Constraints

Start Over You searched for: Descriptor "MHBD deficiency" Remove constraint Descriptor: "MHBD deficiency" Publisher wiley-blackwell Remove constraint Publisher: wiley-blackwell
1 results on '"MHBD deficiency"'

Search Results

1. HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec.

Catalog

Books, media, physical & digital resources