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Letter to the Editor
Mutation of the MMADHC gene in adult-onset cobalamin D deficiency: a report of 2 potentially treatable cases
Mutación del gen MMADHC de la cobalamina D con comienzo en el adulto: a propósito de 2 casos potencialmente tratables
E. Cancho Garcíaa,
Corresponding author
dresthercg@hotmail.com

Corresponding author.
, E. Geánb, B. Oliver Tormoc, A. Torrentsd, E. Esteban Duráne
a Neurologist, Hospital Don Benito-Villanueva de la Serena, Don Benito, Badajoz, Spain
b Clinical Genetics Specialist Consultant, Reference Laboratory Genetics, L’ Hospitalet de Llobregat, Barcelona, Spain
c Pharmacist, Reference Laboratory Genetics, L’ Hospitalet de Llobregat, Barcelona, Spain
d Metabolic Diseases Specialist, Reference Laboratory Genetics, L’ Hospitalet de Llobregat, Spain
e Radiologist, Complejo Hospitalario Infanta Cristina, Badajoz, Spain
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ISSN: 21735808
Original language: English
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