Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B-Reference-Cited by-同舟云学术

Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B

Published:2023-07 Issue:7 Volume:110 Page:1123-1137
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Loftus Stacie K.^ORCID,Gillis Meredith F.,Lundh Linnea,Baxter Laura L.,Wedel Julia C.,Watkins-Chow Dawn E.,Donovan Frank X.,Sergeev Yuri V.,Oetting William S.,Pavan William J.,Adams David R.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference44 articles.

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4. OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24;Kausar;Clin. Genet.,2013

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