Modibo Diallo

Bordeaux, France

Last Updated: 09/26/2026

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Found 8 publications

OCA2 common variant NM_000275.3:c.574-19A>G affects splicing and is pathogenic.

OCA2 common variant NM_000275.3:c.574-19A>G affects splicing and is pathogenic.

Journal: Molecular genetics and metabolism reports

Published: April 23, 2026

Recent advances in albinism.

Recent advances in albinism.

Journal: Presse medicale (Paris, France : 1983)

Published: January 16, 2025

Albinism: from genetics to cell biology and physiopathology.

Albinism: from genetics to cell biology and physiopathology.

Journal: Presse medicale (Paris, France : 1983)

Published: December 27, 2024

A patient with TPCN2-related hypopigmentation and ocular phenotype.

A patient with TPCN2-related hypopigmentation and ocular phenotype.

Journal: European journal of human genetics : EJHG

Published: October 12, 2024

A 65 kilobase deletion of the upstream TYR gene region in a family with oculocutaneous albinism type 1.

A 65 kilobase deletion of the upstream TYR gene region in a family with oculocutaneous albinism type 1.

Journal: Gene

Published: August 27, 2024

Functional Characterization of Splice Variants in the Diagnosis of Albinism.

Functional Characterization of Splice Variants in the Diagnosis of Albinism.

Journal: International journal of molecular sciences

Published: July 02, 2024

Genotypic spectrum of albinism in Mali.

Genotypic spectrum of albinism in Mali.

Journal: Pigment cell & melanoma research

Published: March 13, 2024

BLOC1S5 pathogenic variants cause a new type of Hermansky-Pudlak syndrome.

BLOC1S5 pathogenic variants cause a new type of Hermansky-Pudlak syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 04, 2020

Showing 1-8 of 8

Last Updated: 09/26/2026