Skip to main content
Fig. 1 | BMC Neurology

Fig. 1

From: Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability

Fig. 1

(a) Pedigree of Family A showing the autosomal recessive pattern of ID and presenting the unaffected and affected individuals of the family (A) (b) Pedigree of Family B showing the X-linked pattern of ID and presenting the unaffected and affected individuals of the family (B) Arrows are representing the DNA samples of the individuals submitted for exome sequencing

Back to article page

BMC Neurology

ISSN: 1471-2377

Contact us