Skip to main content
. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: Mol Genet Metab. 2010 Jun 10;101(1):62–65. doi: 10.1016/j.ymgme.2010.05.015

Fig. 1.

Fig. 1

Clinical information of patient with Griscelli Type 2 Syndrome. (A) The pedigree of the proband’s (P) family shows consanguinity arising from a marriage of second cousins. (p = pregnancy; n = multiple siblings, number unknown) (B) The silvery hair of the patient with GS2 shows characteristic pigment clumping (right) compared to a hair of an unaffected dark haired person (left). Sizebar, 50 µm.